# Bridger Biomed, Inc.

- Location (FDA's records): Bozeman, MT
- FDA decisions: 7 (1997–2001): 7 510(k) clearances
- Product codes: FTL (4), DXZ (2), GXQ (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K003906: Modification to Flurotex Surgical Mesh (Jan 26, 2001)
- K003917: Modification to Fluorotex II Surgical Mesh (Jan 26, 2001)
- K002351: Fluorotex II Surgical Mesh (Aug 26, 2000)
- K994032: Fluoro-Tex Cardiovascular Patch (Jul 7, 2000)
- K984197: Fluorotex Surgical Mesh (Jan 7, 1999)
- K980548: Dura-Patch Model DP-XXX (May 13, 1998)
- K973178: Fluoro-Tex Surgical Membrane (Nov 24, 1997)

Source page: https://510kreport.com/company/bridger-biomed