# Ti-Mesh, Inc.

- Location (FDA's records): Las Vegas, NV
- FDA decisions: 3 (1992–1993): 3 510(k) clearances
- Product codes: JEY (2), FTM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Bioplate, Inc.: 8 (https://510kreport.com/company/bioplate)
- Medtronic Neurosurgery: 1 (https://510kreport.com/company/medtronic-neurosurgery)
- Pacific Materials and Interfaces: 1 (https://510kreport.com/company/pacific-materials-and-interfaces)
- Imtec Corp.: 1 (https://510kreport.com/company/imtec)

## Its most-cited devices
- K923419: Tismesh System (1993), cited by 6
- K923802: Timesh Titanium Mini-Softplate/Screw (1992), cited by 4
- K922308: Tilghman Titanium Mesh Skeletal Orbit Liner (1993), cited by 1

## Recent decisions
- K923419: Tismesh System (Apr 8, 1993)
- K922308: Tilghman Titanium Mesh Skeletal Orbit Liner (Jan 12, 1993)
- K923802: Timesh Titanium Mini-Softplate/Screw (Oct 26, 1992)

Source page: https://510kreport.com/company/ti-mesh