Not currently registered with FDA under this name
Ti-Mesh, Inc.
Las Vegas, NV, United States. Named as applicant on 2 dental 510(k) clearances between 1992 and 1993. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 21992–1993
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Ti-Mesh, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 8 Apr 1993 | K923419 | TISMESH SYSTEM | JEY Bone Plate |
| 26 Oct 1992 | K923802 | TIMESH TITANIUM MINI-SOFTPLATE/SCREW | JEY Bone Plate |
Some of these clearances are listed with FDA today by another company: Medtronic, Inc. (2).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.