This presentation contains "forward-looking statements," which are statements related to events, results, activities or developments that SI-BONE expects, believes or anticipates will or may occur in the future. Forward-looking often contain words such as "intends," "estimates," "anticipates," "hopes," "projects," "plans," "expects," "seek," "believes," "see," "should," "will," "would," "target," and similar expressions and the negative versions thereof. Such statements are based on SI-BONE's experience and perception of current conditions, trends, expected future developments and other factors it believes are appropriate under the circumstances, and speak only as of the date made. Forward-looking statements are inherently uncertain and actual results may differ materially from assumptions, estimates or expectations reflected or contained in the forward-looking statements as a result of various factors. For details on the uncertainties that may cause our actual results to be materially different than those expressed in our forward-looking statements, please review our most recent Annual Report on Form 10-K and Quarterly Report on Form 10-Q, especially the information contained in the section captioned "Risk Factors". We undertake no obligation to publicly update or revise any forward-looking statements to reflect new information or future events or otherwise unless required by law.
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Transforming & Leading the Sacropelvic Space
Market
Differentiated
Clinical and
Expanding
Leadership
Platform
Educational Focus
Addressable Markets
$2.4B U.S. annual SIJF
5-year SIJF clinical data
SI-BONE SImulator™
Trauma pelvic ring fracture
opportunity
advanced training platform
solution
279K U.S. annual SIJF
Universal U.S. SIJF payor
>2,800 surgeons performed
$350M U.S. annual trauma
procedures opportunity
coverage
procedure since inception
opportunity2
>70,000 procedures
160+ dedicated field
~200 academic programs
Adult deformity spino-
worldwide since inception
representatives
with training events
pelvic fixation/fusion
Majority U.S. SIJF market
Sacropelvic product
~1,100 trained fellows
$250M U.S. annual
share1
portfolio & pipeline
and residents
deformity opportunity2
Spinemarket, Inc. (2021)
Based on management estimate.
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Setup to Deliver Strong and Sustainable Long-term Growth
▪ iFuse launch
▪
iFuse-TORQlaunch
▪
iFuse Bedrock Granite - FDA BDD
▪
Bedrock launch
▪
SALLY Clinical Trial (2-yrdata)
iFuse 3D launch
LOIS clinical Trial (5-yrdata)
2009
2015
2017
2018
2019
2020
2021
2022
▪ SIFI Clinical Trial
IPO
▪ SI SImulator introduced
▪ iFuse Bedrock Granite -
▪ INSITE Clinical Trial
Product / solutions launched
Clinical trial results
launch & NTAP
▪ iFuse-TORQ - fragility fracture FDA clearance
Near Universal coverage in the U.S. for MIS SIJF
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Second Quarter of 2022 Performance Summary
$25.6M
~86%
ACTIVE SURGEON BASE
720
WORLDWIDE
GROSS
REVENUE
MARGIN
~15%
160+
640
YTD R&D
DEDICATED
INVESTMENT 1
SALES FORCE
2Q21
2Q22
Note: As of quarter ended June 30, 2022. 1. As a percent of YTD revenue
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SI-BONE Inc. published this content on 08 August 2022 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 08 August 2022 21:24:06 UTC.
SI-BONE, Inc. is a medical device company dedicated to solving musculoskeletal disorders of the sacropelvic anatomy. The Company specializes in minimally invasive surgical implant systems to address sacroiliac joint dysfunction as well as address unmet clinical needs in pelvic fixation and management of pelvic fractures. The Company's products include a series of patented titanium implants and the instruments used to implant them, as well as implantable bone products. Its products include iFuse, iFuse-3D, iFuse-TORQ and iFuse Bedrock Granite. Within the United States, iFuse, iFuse-3D and iFuse-TORQ have clearances for applications across sacroiliac joint dysfunction and fusion, adult spinal deformity and degeneration, and pelvic trauma. Its first-generation iFuse, a machined triangular titanium implant, has a triangular cross section that resists twisting or rotation of the implant. The Company's second generation iFuse product, the iFuse-3D implant, is a patented titanium implant.