- A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.
Sintx Technologies, led by CTO Ryan Bock, has achieved FDA clearance and collaborated with a research group at Virginia Tech.
2 reports, 1 independent
Updated Sep 3
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New informationRepeats or wire copies
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What happened
Sintx Technologies, led by CTO Ryan Bock, has achieved FDA clearance and collaborated with a research group at Virginia Tech.
Who's involved
What this event is mainly aboutHow it developed
Newest first. Tap a step to see who reported it.- Sintx Technologies submitted a 510(k) premarket notification to the FDA on July 22, 2025.Sub-event
Sintx Technologies is an FDA-cleared manufacturer that collaborated with Virginia Tech.1 source
NIH provided support for a research study conducted by Sintx Technologies.1 source
Keep exploring
Part of
A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.Also in this story
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- A company plans to submit regulatory applications to the FDA, EMA, and Australian TGA.
- Approval leads to procurement process initiation.
- UroGen Pharma Ltd., headquartered in Princeton, is seeking FDA approval for its products for the U.S. market.
The entities involved
Coverage
Newest first; wire copies grouped- GlobeNewswireSINTX Technologies Publishes Landmark Study Demonstrating Broad-Spectrum Antiviral Activity of Silicon Nitride Breakthrough findings open doors to multi-billion-dollar infection-control markets SALT
- GlobeNewswireSINTX Technologies Expands Silicon Nitride Platform into Hybrid CFR-PEKK Trauma Plates SALT LAKE CITY, Utah, Aug. 04, 2025 (GLOBE NEWSWIRE) -- SINTX Technologies, Inc. (NASDAQ: SINT) (“SINTX” or the