# Biomet Manufactuting Corp.

- Location (FDA's records): Warsaw, IN
- FDA decisions: 2 (2012–2014): 2 510(k) clearances
- Product codes: MBF (1), LPH (1)
- Predicates its devices cite: 3 (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
- Biomet Orthopedics, Inc.: 1 (https://510kreport.com/company/biomet-orthopedics)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)

## Firms that cite its devices most
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)

## Its most-cited devices
- K123297: Compress Segmental Humeral Replacement System (2012), cited by 1

## Recent decisions
- K142746: G7 Finned Acetabular Shell (Dec 29, 2014)
- K123297: Compress Segmental Humeral Replacement System (Nov 20, 2012)

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