# Zimmer Biomet

- Location (FDA's records): Warsaw, IN
- FDA decisions: 6 (2024–2026): 6 510(k) clearances
- Product codes: HSX (1), LZO (1), MBH (1), JDI (1), HRS (1), LPH (1)
- 510(k) review time since 2016: median 60 days, against 90 for FDA's reviews in the same codes and years (4 of 5 faster)
- Predicates its devices cite: 9 (0 its own); citations of its devices by later devices: 1 (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
- Zimmer, Inc.: 7 (https://510kreport.com/company/zimmer)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)

## Firms that cite its devices most
- Howmedica Osteonics Corp., Dba Stryker Orthopaedics: 1 (https://510kreport.com/company/howmedica-osteonics-dba-stryker-orthopaedics)

## Its most-cited devices
- K243293: Zimmer® Persona® Personalized Knee System (2024), cited by 1

## Recent decisions
- K261453: G7® Acetabular System (Sep 23, 2026)
- K251834: Persona Partial Knee (Aug 15, 2025)
- K243571: Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained Liners (Jul 31, 2025)
- K251620: A.L.P.S. Proximal Humerus Plating System (Jul 25, 2025)
- K250834: Zimmer Biomet Ceramic Heads (22.2mm diameter) (Apr 18, 2025)
- K243293: Zimmer® Persona® Personalized Knee System (Dec 20, 2024)

Source page: https://510kreport.com/company/zimmer-biomet