Medical Device Manufacturer · US , Las Vegas , NV

Ti-Mesh, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1992

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ti-Mesh, Inc. Dental ✕

2 devices

1-2 of 2

Cleared Apr 08, 1993

Cleared Oct 26, 1992

TIMESH TITANIUM MINI-SOFTPLATE/SCREW

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Apr 28, 2026