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SINTX Technologies Submits FDA 510(k) for Silicon Nitride Foot & Ankle Medical Devices Advanced Material Science Meets Surgical Precision in Groundbreaking New Platform in Reconstructive Foot & Ankl

Key Takeaway: SINTX Technologies has submitted a 510(k) premarket notification to the FDA for its silicon nitride osteotomy wedges, marking its entry into the reconstructive foot and ankle market. The company emphasizes the advanced biomaterial's benefits, including improved bone integration and reduced infection rates, as well as proprietary implant designs aimed at enhancing surgical efficiency. This development is projected to drive significant revenue growth, with expectations for strong early adoption by healthcare providers. However, the company acknowledges that the approval process and commercialization may encounter uncertainties.

Market Sentiment Analysis

POSITIVE FACTORS

  • SINTX's silicon nitride implants demonstrate superior osteogenic properties, potentially improving patient outcomes.
  • The FDA submission signifies SINTX's entry into a lucrative market expected to grow to $1.38 billion by 2032.
  • Innovative design and single-use instrumentation are intended to enhance surgical efficiency and patient safety.

CONCERNS & RISKS

  • The statement includes forward-looking claims that are subject to market uncertainties and risks.
  • Challenges in the commercialization of new ceramic technologies may pose a risk to successful product launch.
  • Dependence on achieving FDA approval could impact the timeline for market entry.

Full Press Release Details

Technologies Submits FDA 510(k) for Silicon Nitride Foot & Ankle Medical Devices
Material Science Meets Surgical Precision in Groundbreaking New Platform in Reconstructive Foot & Ankle Surgery Market
LAKE CITY, Utah - July 22, 2025 - SINTX Technologies, Inc. (NASDAQ: SINT) ("SINTX" or the "Company"),
an advanced ceramics innovator specializing in silicon nitride (Si N ) for medical applications, today announced the submission
of a 510(k) premarket notification to the U.S. Food and Drug Administration (FDA) for its novel silicon nitride osteotomy wedges-marking
the official entry into the foot and ankle reconstruction market. These next-generation implants blend cutting-edge biomaterials science
with surgical precision and are designed to elevate standards in orthopedic procedures.
devices are manufactured from SINTX's proprietary medical-grade silicon nitride, a biomaterial with a proven clinical track record
of over 50,000 spinal interbody fusion devices implanted since 2008. With this submission, SINTX is extending the success of Si N
beyond the spine and into the global foot and ankle fusion market, currently valued at approximately $750.5 million and which is expected
to grow to $1.38 billion by 2032 according to industry research.
Advantages of Silicon Nitride
a clinical standpoint, Si N is uniquely positioned among biomaterials to solve several of the most pressing challenges in
orthopedic reconstruction:
Pro-osteogenic : Unlike PEEK or titanium, Si N has been shown to actively promote bone cell adhesion, proliferation, and differentiation. In vivo and in vitro studies have shown enhanced osseointegration and fusion potential due to the material's inherent surface chemistry and nanotopography.
Antimicrobial Without Additives : Si N has been shown to inhibit bacterial colonization and proliferation-including several antibiotic-resistant strains -through inherent surface chemistry without a supplemental coating. This is particularly critical in foot and ankle procedures where occurrences of hardware-related infections persist despite current best practices.
Radiographic Clarity : Si N implants are intrinsically radiolucent with clearly visible boundaries on X-ray and CT scans. This facilitates precise intraoperative placement and clear post-operative evaluation of bone healing-unlike metal implants which obscure fusion assessment.
believe Si N is the ideal orthopedic biomaterial for fusion procedures where infection risk, healing rate, and long-term
stability are paramount," said Eric Olson, CEO of SINTX Technologies.
Innovation: Proprietary Designs with Disposable Instrumentation
parallel with biomaterial excellence, SINTX has engineered proprietary implant geometries and disposable instrumentation to elevate surgical
Implant Geometry : The family of wedges were developed in collaboration with leading foot and ankle surgeons to optimize for biomechanical correction, surface area contact, and ease of insertion.
Disposable Instrument Set : At full launch we anticipate each implant system to be paired with a sterile, single-use instrument kit to enhance maximum surgical efficiency and sterility. This potentially leads to a reduction in intraoperative delays, elimination of reprocessing errors, and a decrease in OR turnover time-benefits that hospitals and ambulatory surgery centers alike will value.
combined the novel clinical advantages of silicon nitride with intuitive implant designs and single-use instrumentation to deliver a
truly differentiated solution," said Lisa Marie Del Re, Chief Commercial Officer of SINTX Technologies. "This approach goes
beyond innovation in material science. We've reimagined the surgical experience, striving to improve outcomes, enhance efficiency,
and deliver stronger economic value across the care continuum."
Launch and Financial Outlook
The FDA submission is backed by over a decade of clinical and preclinical data on SINTX's Si N biomaterial, including peer-reviewed publications, biocompatibility studies, and documented fusion success.
With compelling clinical advantages and meaningful input from high-volume reconstructive surgeons, the company anticipates strong early adoption of its foot and ankle portfolio. This launch represents a key growth catalyst for SINTX, with the potential to drive meaningful revenue through broader market penetration and increasing procedural demand across both hospital and ambulatory surgery center settings.
Value to All Stakeholders
For Patients : The design and material properties of our silicon nitride implants are intended to support successful bone fusion and to reduce infection risk; key considerations in recovery and long-term outcomes.
For Surgeons : Engineered for enhanced intraoperative visualization and ease of use, our system integrates advanced implant geometry with streamlined instrumentation to support surgical precision and procedural consistency.
For Providers and Stakeholders : The combination of sterile, single-use kits and differentiated biomaterial technology offers operational efficiencies and clinical distinction, positioning this platform for strong alignment with evolving value-based care models and increased procedural demand.
is not just another foot fusion product line-this is a platform," added Olson. "A platform built on a proven material,
rooted in over a decade of clinical experience, and refined with thoughtful surgical design. We believe SINTX is redefining what's
possible in orthopedic advancements."
implants will be manufactured at SINTX Technologies FDA audited and ISO certified manufacturing facility and distributed under the company
name SiNAPTIC Surgical. SiNAPTIC was acquired by SINTX on July 1, 2025.
more information, visit www.sintx.com or www.sinaptic.com
SINTX Technologies, Inc.
in Salt Lake City, Utah, SINTX Technologies is an advanced ceramics company that develops and commercializes materials, components, and
technologies for medical and agribiotech applications. SINTX is a global leader in the research, development, and manufacturing of silicon
nitride, and its products have been implanted in humans since 2008. Over the past several years, SINTX has utilized strategic acquisitions
and alliances to enter new markets. For more information on SINTX Technologies or its materials platform, visit www.sintx.com.
press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 ("PSLRA")
that are subject to a number of risks and uncertainties. Forward-looking statements can be identified by words such as: "anticipate,"
"believe," "project," "estimate," "expect," "strategy," "future,"
"likely," "may," "should," "will" and similar references to future periods.
are cautioned not to place undue reliance on the forward-looking statements, which speak only as of the date on which they are made and
reflect management's current estimates, projections, expectations and beliefs. Because forward-looking statements relate to the
future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which
are outside of our control. Forward-looking statements in this press release include our anticipation that there will be strong early
adoption of our foot and ankle portfolio, that the product launch will represent a key growth catalyst for SINTX, with the potential
to drive meaningful revenue through broader market penetration and increasing procedural demand across both hospital and ambulatory surgery
center settings. Our actual results and financial condition may differ materially from those indicated in the forward-looking statements.
Important factors that could cause our actual results and financial condition to differ materially from those indicated in the forward-looking
statements include, among others, difficulty in commercializing ceramic technologies and development of new product opportunities. A
discussion of other risks and uncertainties that could cause our actual results and financial condition to differ materially from those
indicated in the forward-looking statements can be found in SINTX's Risk Factors disclosure in its Annual Report on Form 10-K,
filed with the SEC on March 19, 2025, and in SINTX's other filings with the SEC. SINTX undertakes no obligation to publicly revise
or update the forward-looking statements to reflect events or circumstances that arise after the date of this report, except as required
and Media Inquiries for SINTX:

Frequently Asked Questions

What new devices did SINTX Technologies submit to the FDA?

SINTX Technologies submitted a 510(k) for novel silicon nitride osteotomy wedges.

What advantages does silicon nitride offer in orthopedic surgery?

Silicon nitride promotes bone cell activity, inhibits infections, and offers clear imaging.

How does SINTX's innovation improve surgical procedures?

SINTX has developed proprietary implant designs and disposable instruments for efficiency.

What is the expected growth of the foot and ankle fusion market?

The market is projected to grow from $750.5 million to $1.38 billion by 2032.

What benefits do SINTX implants offer patients and surgeons?

They support bone fusion, reduce infection risk, and enhance surgical precision.

Last updated: Jul 22, 2025