# Nexus CMF, LLC

- Location (FDA's records): Golden
- FDA decisions: 3 (2001–2026): 1 510(k) clearance and 2 original PMA approvals
- Product codes: MPI (1), LZD (1), HRX (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
- K260156: TruVision Single-Use 1.9mm Arthroscopy System (Oct 9, 2026)
- P000035: TMJ Fossa-Eminence Prosthesis (TM) (Feb 27, 2001)
- P000023: TMJ Fossa-Eminence/Condylar Prostheses (Jan 5, 2001)

Source page: https://510kreport.com/company/nexus-cmf