# Lincotek Medical

- Location (FDA's records): Bartlett, TN
- FDA decisions: 2 (2025–2026): 2 510(k) clearances
- Product codes: ODP (1), HTN (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Globus Medical, Inc.: 2 (https://510kreport.com/company/globus-medical)
- Elevation Spine: 1 (https://510kreport.com/company/elevation-spine)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)

## Recent decisions
- K252081: SportLinc Syndesmosis Device (Mar 27, 2026)
- K250764: SpineLinc Anterior Cervical Implant System (Dec 5, 2025)

Source page: https://510kreport.com/company/lincotek-medical