You should read the following discussion and analysis of our financial condition
and results of operations together with our unaudited condensed consolidated
financial statements and related notes included in this Quarterly Report on Form
10-Q and our audited financial statements and related notes thereto for the year
ended December 31, 2019, included in our prospectus dated May 21, 2020 filed
with the U.S. Securities and Exchange Commission, pursuant to Rule 424(b)(4)
under the Securities Act.

Overview

We are a commercial-stage medical device company focused on developing products
to treat and transform the lives of patients suffering from venous diseases. Our
initial product offering consists of two minimally-invasive, novel
catheter-based mechanical thrombectomy devices. We purpose-built our products
for the specific characteristics of the venous system and the treatment of the
two distinct manifestations of venous thromboembolism, or VTE - deep vein
thrombosis and pulmonary embolism. Our ClotTriever product is FDA-cleared for
the removal of clot from peripheral blood vessels and is used to treat patients
suffering from deep vein thrombosis, or DVT. Our FlowTriever product is the
first thrombectomy system FDA-cleared for the treatment of pulmonary embolism,
or PE.

We believe the best way to treat VTE and improve the quality of life of patients
suffering from this disease is to safely and effectively remove the blood clot.
With that in mind, we designed and purpose-built our ClotTriever and FlowTriever
products to remove large clots from large vessels and eliminate the need for
thrombolytic drugs. We believe our products are transformational and could be
the catalyst to drive an evolution of treatment for venous diseases,
establishing our products as the standard of care for DVT and PE.

We believe our venous-focused commercial organization provides a significant
competitive advantage. Our most important relationships are between our sales
representatives and our target physicians, which include interventional
cardiologists, interventional radiologists and vascular surgeons. We have
developed systems and processes to harness the information gained from these
relationships and we leverage this information to rapidly iterate products,
introduce and execute physician education and training programs and scale our
sales organization. We market and sell our products to hospitals, which are
reimbursed by various third-party payors. We have dedicated meaningful resources
to building a direct sales force in the United States, and we are actively
expanding our sales organization through additional sales representatives and
territories.

On May 27, 2020, we completed our IPO, which resulted in the issuance and sale
of 9,432,949 shares of common stock, including 1,230,384 shares sold pursuant to
the exercise of the underwriters' over-allotment option, at the IPO price of
$19.00 per share. We received net proceeds of approximately $163.0 million from
the IPO, after deducting underwriters' discounts and commissions of $12.6
million and offering costs of $3.7 million.

Prior to our IPO, our primary sources of capital were private placements of
preferred stock, debt financing arrangements and revenue from sales of our
products. Since inception, we have raised a total of approximately $54.2 million
in net proceeds from private placements of preferred stock. As of September 30,
2020, we had cash and cash equivalents of $168.0 million, no long-term debt
outstanding and an accumulated deficit of $34.4 million.

For the three months ended September 30, 2020, we generated revenue of $38.7
million, with a gross margin of 91.7% and net income of $6.5 million, compared
to revenue of $14.2 million, with a gross margin of 89.4% and net income of $0.4
million for the three months ended September 30, 2019.

For the nine months ended September 30, 2020, we generated revenue of $91.1
million, with a gross margin of 89.7% and net income of $6.8 million, compared
to revenue of $31.2 million, with a gross margin of 87.9% and net loss of $1.6
million for the nine months ended September 30, 2019.

COVID-19



In December 2019, a novel strain of coronavirus, SARS-CoV-2, was identified in
Wuhan, China. Since then, SARS-CoV-2, and the resulting disease, COVID-19, has
spread to most countries, including all 50 states in the United States. In
response to the pandemic, numerous state and local jurisdictions imposed, and
others in the future may impose, "shelter-in-place" orders, quarantines,
executive orders and similar government orders and restrictions for their
residents to control the spread of COVID-19. For example, in the United States,
governmental authorities recommended, and in certain cases required, that
elective, specialty and other procedures and appointments be suspended or
canceled to avoid non-essential patient exposure to medical environments and
potential infection with COVID-19 and to focus limited resources and personnel
capacity toward the treatment of COVID-19 patients. Similarly, on March 19,
2020, the governor of California, where our headquarters are located, issued
"stay at home" orders limiting non-essential activities, travel and business
operations. Such orders or restrictions resulted in reduced operations at our
headquarters (including our manufacturing facility), work stoppages, slowdowns
and delays, travel restrictions and cancellation of events. These orders and
restrictions significantly decreased the number of procedures performed using
our products during March and April 2020 and otherwise negatively impacted our
operations, including new customer procurement and onboarding.

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In response to the impact of COVID-19, we implemented a variety of measures to
help us manage through its impact and position us to resume operations quickly
and efficiently once these restrictions were lifted. These measures existed
across several operational areas and included:



        • Continuing to build our team, including identifying and
          recruiting our next group of new sales representatives;


        • Enhancing our physician outreach and training with the
          launch of our Clot Warrior Academy consisting of a series of
          live webinars and an online education portal;

• Continuing to support procedures using our products both in-person and


          virtually;


        • Adapting, expanding and improving our sales training
          programs and customer engagement to address the current
          environment;

• Continuing to expand our engineering infrastructure and focusing on


          organic opportunities;


        • Producing approximately four months' worth of inventory
          before temporarily suspending production in April 2020;


        • Continuing to protect and support our employees, including no
          layoffs, furloughs or compensation reductions to date;


        • Executing a successful work-from-home strategy for
          administrative functions that includes launching various
          efficiency projects in information technology, accounting
          and operations;

• Monitoring and reviewing recent case studies of VTE patients suffering


          from COVID-19;


        • Initiating market assessment and commercial entry planning for our
          international expansion; and


        • Accessing the remaining $10.0 million on our term loan on March 23,
          2020, which was repaid in full along with all our long term-debt in
          August 2020.


Despite the negative impacts from COVID-19, for the nine months ended September
30, 2020, approximately 8,600 procedures were performed using our products,
compared to approximately 2,800 procedures in the nine months ended September
30, 2019. During the second quarter, we experienced disruptions to our procedure
volume beginning in mid-March as a result of COVID-19, and weekly procedure
volumes declined by approximately 40% by mid-April when compared to weekly
procedure volumes in early March. The decrease in procedure volume impacted DVT
procedures and PE procedures relatively equally, with both types of procedures
declining during this period. However, we saw a recovery in procedure volume in
June that was higher than our pre COVID-19 peak. During the third quarter, we
saw continued sequential growth beyond previous quarters.

While we are encouraged by our third quarter results, we are aware that the
actual and perceived impact of COVID-19 is changing and cannot be predicted. As
a result, we cannot assure you that our recent procedure volumes are indicative
of future results or that we will not experience additional negative impacts
associated with COVID-19, which could be significant. The COVID-19 pandemic has
negatively impacted our business, financial condition and results of operations
by significantly decreasing and delaying the number of procedures performed
using our products, and we expect the pandemic could continue to negatively
impact our business, financial condition and results of operations.

Procedure Volume



We regularly review various operating and financial metrics to evaluate our
business, measure our performance, identify trends affecting our business,
formulate our business plan and make strategic decisions. We believe the number
of procedures performed to treat DVT and PE using our products is an indicator
of our ability to drive adoption and generate revenue. We believe this is an
important metric for our business; however, we anticipate that additional
metrics may become important as our business grows. The following table lists
the number of procedures performed in each of the three-month periods as
indicated:



                                                                       Three Months Ended
                        Sept 30,                          March 31,      Dec. 31,      Sept 30,
Procedures(1)             2020         June 30, 2020         2020          2019          2019         June 30, 2019       March 31, 2019
DVT                         2,000            1,400            1,300          1,000          700              500                  300
PE                          1,700            1,100            1,100           800           600              400                  300
                            3,700            2,500            2,400          1,800         1,300             900                  600



(1) We define a procedure as any instance in which a physician treats DVT or PE

using our products. We estimate the number of procedures performed based on

records created by our sales representatives. This metric has limitations as

we only have records for the procedures where our sales representatives have

notice that a procedure has been performed. Revenue is recognized based on

hospital purchase orders, not based on the procedure records created by our


    sales representatives. Numbers are rounded to the nearest hundred.


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Components of our Results of Operations

Revenue



We currently derive all our revenue from the sale of our ClotTriever and
FlowTriever products to hospitals in the United States. Our customers typically
purchase an initial stocking order of our products and then reorder
replenishment product as procedures are performed. No single customer accounted
for 10% or more of our revenue during the three and nine months ended
September 30, 2020 and 2019. For the three and nine months ended September 30,
2020, approximately 54% of our customers used both of our products, 34% used
ClotTriever only and 12% used FlowTriever only. We expect revenue to increase in
absolute dollars as we expand our sales organization and sales territories, add
customers, expand the base of physicians that are trained to use our products,
expand awareness of our products with new and existing customers and as
physicians perform more procedures using our products. Revenue for ClotTriever
and FlowTriever products as a percentage of total revenue is as follows:



                Three Months Ended September 30,           Nine Months Ended September 30,
                  2020                    2019              2020                    2019
ClotTriever              37 %                    38 %              38 %                    38 %
FlowTriever              63 %                    62 %              62 %                    62 %


For the nine months ended September 30, 2020, our blended revenue per procedure
was approximately $9,100. Blended revenue per procedure represents the average
of the average selling price per ClotTriever and the average price per
FlowTriever procedure.

Cost of Goods Sold and Gross Margin



We manufacture and/or assemble all our products at our facility in Irvine,
California. Cost of goods sold consists primarily of the cost of raw materials,
components, direct labor and manufacturing overhead. Overhead costs include the
cost of quality assurance, material procurement, inventory control, facilities,
equipment and operations supervision and management, including stock-based
compensation. Cost of goods sold also includes depreciation expense for
production equipment and certain direct costs such as shipping costs and royalty
expense. Shipping costs billed to customers are reported as a reduction of cost
of goods sold. We expect cost of goods sold to increase in absolute dollars as
our revenue grows and more of our products are sold.

We calculate gross margin as gross profit divided by revenue. Our gross margin
has been and will continue to be affected by a variety of factors, including
average selling prices, product sales mix, production and ordering volumes,
manufacturing costs, product yields, headcount and cost-reduction strategies.
Our gross margin could fluctuate from quarter to quarter as we introduce new
products, and as we adopt new manufacturing processes and technologies.

Treatments using the FlowTriever may involve one or more Triever aspiration
catheters and one or more FlowTriever catheters. We charge customers the same
price for each FlowTriever procedure, regardless of the number of components
used. As a result, changes in the number of components used, the cost of these
components and the introduction of additional components can impact our gross
margin.


Research and Development Expenses



Research and development, or R&D, expenses consist primarily of engineering,
product development, clinical studies to develop and support our products,
regulatory expenses, and other costs associated with products that are in
development. These expenses include employee compensation, including stock-based
compensation, supplies, consulting, prototyping, testing, materials, travel
expenses, depreciation and an allocation of facility overhead expenses.
Additionally, R&D expenses include costs associated with our clinical trials and
registries, including clinical study design, clinical study site initiation and
study costs, data management, and internal and external costs associated with
our regulatory compliance, including the costs of outside consultants and
contractors that assist in the process of submitting and maintaining regulatory
filings. We expense R&D costs as incurred. We expect R&D expenses as a
percentage of revenue to vary over time depending on the level and timing of our
new product development efforts, as well as our clinical development, clinical
trials and registries and other related activities.

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Selling, General and Administrative Expenses



Selling, general and administrative, or SG&A, expenses consist primarily of
compensation for personnel, including stock-based compensation, related to
selling and marketing functions, physician education programs, commercial
operations and analytics, finance, information technology and human resource
functions. Other SG&A expenses include sales commissions, travel expenses,
promotional activities, marketing initiatives, market research and analysis,
conferences and trade shows, physician training, professional services fees
(including legal, audit and tax fees), insurance costs, general corporate
expenses and facilities-related expenses. We expect SG&A expenses to continue to
increase in absolute dollars as we expand our sales and marketing organization
and infrastructure to both drive and support the anticipated growth in revenue
and due to additional legal, accounting, insurance and other expenses associated
with being a public company.

Interest Income

Interest income consists primarily of interest income earned on our cash and cash equivalents.



Interest Expense

Interest expense consists primarily of interest incurred on our outstanding indebtedness and non-cash interest related to the amortization of debt discount and issuance costs associated with our indebtedness.

Change in Fair Value of Warrant Liabilities



Change in fair value of warrant liabilities consists of gains and losses
resulting from the remeasurement of the fair value of our preferred stock
warrant liabilities at each balance sheet date. Upon the closing of our IPO, our
outstanding preferred stock warrants automatically converted into warrants to
purchase shares of our common stock. At such time, the final fair value of the
warrant liability was reclassified to stockholders' equity (deficit). We will no
longer record any related periodic fair value adjustments.

Results of Operations

Comparison of the three months ended September 30, 2020 and 2019



The following table sets forth the components of our unaudited statements of
operations in dollars and as percentage of revenue for the periods presented
(dollars in thousands):



                                         Three Months Ended September 30,
                                2020           %              2019             %           Change $
Revenue                       $ 38,715          100.0 %    $    14,225         100.0 %    $   24,490
Cost of goods sold               3,228            8.3 %          1,510          10.6 %         1,718
Gross profit                    35,487           91.7 %         12,715          89.4 %        22,772
Operating expenses:
Research and development         5,217           13.5 %          1,722          12.1 %         3,495
Selling, general and
  administrative                23,080           59.6 %         10,100          71.0 %        12,980
Total operating expenses        28,297           73.1 %         11,822          83.1 %        16,475
Income from operations           7,190           18.6 %            893           6.3 %         6,297
Other income (expense)
Interest income                    208            0.5 %             19           0.1 %           189
Interest expense                  (251 )         (0.6 %)          (226 )        (1.6 %)          (25 )
Other expenses                    (651 )         (1.7 %)             -           0.0 %          (651 )
Change in fair value of
  warrant liabilities                -            0.0 %           (320 )        (2.2 %)          320
Total other expenses, net         (694 )         (1.8 %)          (527 )        (3.7 %)         (167 )
Net income and
comprehensive income          $  6,496           16.8 %    $       366           2.6 %    $    6,130




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Revenue. Revenue increased $24.5 million, or 172%, to $38.7 million during the
three months ended September 30, 2020, compared to $14.2 million during the
three months ended September 30, 2019. The increase in revenue was due primarily
to an increase in the number of products sold and an increase in the average
selling prices of our products.

Cost of Goods Sold and Gross Margin. Cost of goods sold increased $1.7 million,
or 114%, to $3.2 million during the three months ended September 30, 2020,
compared to $1.5 million during the three months ended September 30, 2019. This
increase was due to the increase in the number of products sold and additional
manufacturing overhead costs incurred as we invested significantly in our
operational infrastructure to support anticipated future growth. Gross margin
for the three months ended September 30, 2020 increased to 91.7%, compared to
89.4% for the three months ended September 30, 2019, due to an increase in the
average selling prices of our products and improved operating leverage.

Research and Development Expenses. R&D expenses increased $3.5 million, or 203%,
to $5.2 million during the three months ended September 30, 2020, compared to
$1.7 million during the three months ended September 30, 2019. The increase in
R&D expenses was primarily due to increases of $1.6 million of personnel-related
expenses, $0.8 million in materials and supplies, $0.8 million of clinical study
and registry expenses, and $0.2 million in professional fees.

Selling, General and Administrative Expenses. SG&A expenses increased $13.0
million, or 129%, to $23.1 million during the three months ended September 30,
2020, compared to $10.1 million during the three months ended September 30,
2019. The increase in SG&A costs was primarily due to an increase of $10.0
million in personnel-related expenses as a result of increased headcount across
our organization and increased commissions due to higher revenue, an increase of
$1.0 million in professional fees, an increase of $1.0 million in insurance
costs, and an increase of $0.3 million in facility costs.

Interest Income. Interest income increased by $189,000 to $208,000 during the
three months ended September 30, 2020, compared to $19,000 during the three
months ended September 30, 2019. The increase in interest income was primarily
due to an increase in average cash and cash equivalents during the three months
ended September 30, 2020, compared to the three months ended September 30, 2019.

Interest Expense. Interest expense increased by $25,000 or 11% during the three
months ended September 30, 2020, compared to the three months ended
September 30, 2019, due primarily to the higher average borrowings during the
three months ended September 30, 2020.

Change in Fair Value of Warrant Liabilities. We recorded no change in fair value
of warrant liabilities for the three months ended September 30, 2020, compared
to $0.3 million for three months ended September 30, 2019.

Other expenses. Other expenses for the three months ended September 30, 2020
consisted primarily of a $0.7 million loss on extinguishment of debt related to
the payoff of our debt facility with Signature Bank.

Comparison of the nine months ended September 30, 2020 and 2019



The following table sets forth the components of our unaudited statements of
operations in dollars and as percentage of revenue for the periods presented
(dollars in thousands):

                                         Nine Months Ended September 30,
                                2020           %              2019             %           Change $
Revenue                       $ 91,059          100.0 %    $    31,242         100.0 %    $   59,817
Cost of goods sold               9,420           10.3 %          3,772          12.1 %         5,648
Gross profit                    81,639           89.7 %         27,470          87.9 %        54,169
Operating expenses:
Research and development        11,863           13.0 %          4,511          14.4 %         7,352
Selling, general and
  administrative                58,353           64.1 %         23,328          74.7 %        35,025
Total operating expenses        70,216           77.1 %         27,839          89.1 %        42,377
Income (loss) from
operations                      11,423           12.6 %           (369 )        (1.2 %)       11,792
Other income (expense)
Interest income                    409            0.4 %             66           0.2 %           343
Interest expense                (1,060 )         (1.2 %)          (682 )        (2.2 %)         (378 )
Other expenses                    (651 )         (0.7 %)             -           0.0 %          (651 )
Change in fair value of
  warrant liabilities           (3,317 )         (3.6 %)          (562 )        (1.8 %)       (2,755 )
Total other expenses, net       (4,619 )         (5.1 %)        (1,178 )        (3.8 %)       (3,441 )
Net income (loss) and
comprehensive income (loss)   $  6,804            7.5 %    $    (1,547 )        (5.0 %)   $    8,351


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Revenue. Revenue increased $59.8 million, or 192%, to $91.1 million during the
nine months ended September 30, 2020, compared to $31.2 million during the nine
months ended September 30, 2019. The increase in revenue was due primarily to an
increase in the number of products sold and an increase in the average selling
prices of our products. The increase in revenue was offset in part by the
negative impact of the COVID-19 pandemic on procedure volume and new orders
during the nine months ended September 30, 2020.

Cost of Goods Sold and Gross Margin. Cost of goods sold increased $5.6 million,
or 150%, to $9.4 million during the nine months ended September 30, 2020,
compared to $3.8 million during the nine months ended September 30, 2019. This
increase was due to the increase in the number of products sold and additional
manufacturing overhead costs incurred as we invested significantly in our
operational infrastructure to support anticipated future growth. Cost of goods
sold for the nine months ended September 30, 2020 was also impacted by $1.1
million in idle production capacity costs associated with the COVID-19 pandemic.
Gross margin for the nine months ended September 30, 2020 increased to 89.7%,
compared to 87.9% for the nine months ended September 30, 2019 due to an
increase in the average selling prices of our products and improved operating
leverage.

Research and Development Expenses. R&D expenses increased $7.4 million, or 163%,
to $11.9 million during the nine months ended September 30, 2020, compared to
$4.5 million during the nine months ended September 30, 2019. The increase in
R&D expenses was primarily due to increases of $3.1 million of personnel-related
expenses, $1.9 million of clinical study and registry expenses, $1.8 million in
materials and supplies, and $0.3 million in professional fees.

Selling, General and Administrative Expenses. SG&A expenses increased $35.0
million, or 150%, to $58.4 million during the nine months ended September 30,
2020, compared to $23.3 million during the nine months ended September 30, 2019.
The increase in SG&A costs was primarily due to an increase of $27.8 million in
personnel-related expenses as a result of increased headcount across our
organization and increased commissions due to higher revenue, an increase of
$2.7 million in professional fees, an increase of $1.4 million in insurance
costs, an increase of $0.7 million in facility costs, and an increase in $0.6
million in travel costs.

Interest Income. Interest income increased by $343,000 to $409,000 during the
nine months ended September 30, 2020, compared to $66,000 during the nine months
ended September 30, 2019. The increase in interest income was primarily due to
an increase in average cash and cash equivalents during the nine months ended
September 30, 2020, compared to the nine months ended September 30, 2019.

Interest Expense. Interest expense increased by $0.4 million or 55% during the
nine months ended September 30, 2020, compared to the nine months ended
September 30, 2019. This increase was primarily due to higher average borrowings
under our credit facilities during the nine months ended September 30, 2020.

Change in Fair Value of Warrant Liabilities. Change in fair value of warrant
liabilities increased $2.7 million to $3.3 million for the nine months ended
September 30, 2020, compared to $0.6 million for nine months ended September 30,
2019. This increase was due to the fair value remeasurement of our convertible
preferred stock warrant liabilities.

Other expenses. Other expenses for the nine months ended September 30, 2020 consisted primarily of a $0.7 million loss on extinguishment of debt related to the payoff of our debt facility with Signature Bank.

Liquidity and Capital Resources



To date, our primary sources of capital have been the net proceeds we received
through private placements of preferred stock, debt financing agreements, the
sale of common stock in our IPO, and revenue from the sale of our products. On
May 27, 2020, we completed our IPO, including the underwriters full exercise of
their over-allotment option, selling 9,432,949 shares of our common stock at
$19.00 per share. Upon completion of our IPO, we received net proceeds of
approximately $163.0 million, after deducting underwriting discounts and
commissions and offering expenses. In August 2020, we repaid in full the
$30.0 million of principal owed under the credit facility with Signature
Bank. As of September 30, 2020, we had cash and cash equivalents of
$168 million, and an accumulated deficit of $34.4 million. In September 2020, we
entered into a new revolving Credit Agreement with Bank of America which
provides for loans up to a maximum of $30 million. As of September 30, 2020, we
had no principal outstanding under the Credit Agreement and the amount available
to borrow was approximately $25.2 million.

Based on our current planned operations, we expect that our cash and cash equivalents and available borrowings will enable us to fund our operating expenses for at least 12 months from the date hereof.


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If our available cash balances and anticipated cash flow from operations are
insufficient to satisfy our liquidity requirements including because of lower
demand for our products as a result of the risks described in this Quarterly
Report, we may seek to sell additional common or preferred equity or convertible
debt securities, enter into an additional credit facility or another form of
third-party funding or seek other debt financing. The sale of equity and
convertible debt securities may result in dilution to our stockholders and, in
the case of preferred equity securities or convertible debt, those securities
could provide for rights, preferences or privileges senior to those of our
common stock. The terms of debt securities issued or borrowings pursuant to a
credit agreement could impose significant restrictions on our operations. If we
raise funds through collaborations and licensing arrangements, we might be
required to relinquish significant rights to our platform technologies or
products or grant licenses on terms that are not favorable to us. Additional
capital may not be available on reasonable terms, or at all.

Cash Flows



The following table summarizes our cash flows for each of the nine-month periods
indicated (in thousands):



                                               Nine Months Ended September 30,
                                                  2020                  2019
      Net Cash (used in) provided by:
      Operating activities                  $          3,536       $       (4,110 )
      Investing activities                            (3,076 )             (2,062 )
      Financing activities                           143,889               

198

Net increase (decrease) in cash


        and cash equivalent                 $        144,349       $       (5,974 )

Net Cash Used in Operating Activities



Net cash provided by operating activities for the nine months ended
September 30, 2020 was $3.5 million, consisting primarily of net income of $6.8
million and non-cash charges of $7.0 million, offset by an increase in net
operating assets of $10.3 million. The increase in net operating assets was
primarily due to increases in accounts receivable of $9.6 million and
inventories of $3.2 million to support the growth of our operations, an increase
in prepaid and other assets of $2.9 million primarily from prepaid insurance,
which were partially offset by increases in accounts payable of $1.0 million and
accrued liabilities of $4.5 million due to timing of payments and growth of our
operations. The non-cash charges primarily consisted of $3.3 million in change
in fair value of the preferred stock warrant liabilities, stock-based
compensation of $2.0 million, $0.9 million in depreciation, and $0.6 million in
loss on extinguishment of debt.

Net cash used in operating activities for the nine months ended September 30,
2019 was $4.1 million, consisting primarily of a net loss of $1.5 million and an
increase in net operating assets of $3.9 million, partially offset
by non-cash charges of $1.3 million. The increase in net operating assets was
primarily due to an increase in accounts receivable of $5.7 million due to
increase in sales and inventories of $2.0 million to support the growth of our
operations, partially offset by increases in account payable of $1.0 million and
accrued liabilities of $3.1 million due to timing of payments and growth of our
operations. Non-cash charges consisted primarily of $0.4 million in
depreciation, stock-based compensation of $0.3 million, and the change in fair
value of the convertible preferred stock warrants of $0.6 million.

Net Cash Used in Investing Activities



Net cash used in investing activities in the nine months ended September 30,
2020 and 2019 was $3.1 million and $2.1 million, respectively, consisting of
purchases of property and equipment.

Net Cash Provided by Financing Activities



Net cash provided by financing activities in the nine months ended September 30,
2020 was $143.9 million primarily consisting of net IPO proceeds of $164.4
million and net proceeds of $10.0 million received from additional borrowings
under the credit facility with Signature Bank, partially offset by the $30.3
million repayment of the amount outstanding under the credit facility.

There were no significant cash flow financing activities in the nine months ended September 30, 2019.


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Off-Balance Sheet Arrangements



We do not have any off-balance sheet arrangements, as defined by applicable
regulations of the U.S. Securities and Exchange Commission, that are reasonably
likely to have a current or future material effect on our financial condition,
results of operations, liquidity, capital expenditures or capital resources.

Contractual Obligations and Commitments



There have been no material changes outside the ordinary course of business
to the Company's contractual obligations from those disclosed in "Management's
Discussion and Analysis of Financial Condition and Results of Operations"
included in the prospectus dated May 21, 2020 filed with the U.S. Securities and
Exchange Commission pursuant to Rule 424(b)(4) under the Securities Act.

Critical Accounting Policies and Estimates



Management's discussion and analysis of our financial condition and results of
operations is based on our financial statements, which have been prepared in
accordance with U.S. GAAP. The preparation of these financial statements
requires us to make estimates and assumptions for the reported amounts of
assets, liabilities, revenue, expenses and related disclosures. Our estimates
are based on our historical experience and on various other factors that we
believe are reasonable under the circumstances, the results of which form the
basis for making judgments about the carrying value of assets and liabilities
that are not readily apparent from other sources. Actual results may differ from
these estimates under different assumptions or conditions and any such
differences may be material.

There were no material changes to our critical accounting policies or in the
methodology used for estimates from those described in "Management's Discussion
and Analysis of Financial Condition and Results of Operations" included in the
Prospectus.

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