# Biomet, Inc. (manufacturer, Warsaw, IN): 18 new FDA device listings, incl. prosthesis, hip, semi-constrained, metal/polymer, porous uncemented

**Score:** 95/100

| Field | Value |
|---|---|
| Establishment | Biomet, Inc. |
| Owner / operator | Zimmer Inc |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Warsaw, IN, US |
| New listings | 18 |
| Devices | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer; Hip, Semi-Constrained, Cemented, Metal/Polymer + Additive, Cemented; Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented; Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented; Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer |
| Product codes | LPH, JDI, KRO, OQH, OQG, LZO, OQI, MAY, KWY, KWZ, MEH, OJH |
| Device classes | Class I, Class II |
| Medical specialties | Orthopedic, General, Plastic Surgery |
| Brand names | Zimmer Biomet OSS Orthopedic Salvage System OsseoTi Sleeves and Augments; G7 Acetabular System; OSSTM Orthopedic Salvage System; Taperloc Complete Hip Stem; SCP Convenience Kits |
| First new listing | 2026-06-04 |
| Latest new listing | 2026-09-24 |
| FDA registration number | 1825034 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
- Listed in the last 45 days.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.