# Changzhou Biomet Medical Devices Co., Ltd. (contract manufacturer, Changzhou City Jiangsu, CN): 8 new FDA device listings, incl. plate, bone

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Changzhou Biomet Medical Devices Co., Ltd. |
| Owner / operator | Zimmer Inc |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device |
| Location | Changzhou City Jiangsu, CN |
| New listings | 8 |
| Devices | Plate, Bone; Screw, Fixation, Intraosseous; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented; Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer; Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate; Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented |
| Product codes | JEY, DZL, MAY, LPH, KWY, KWZ, MEH, OQG |
| Device classes | Class II |
| Medical specialties | Dental, Orthopedic |
| Brand names | Biomet Microfixation OmniMax MMF System; Taperloc Complete Hip Stem |
| First new listing | 2026-06-04 |
| Latest new listing | 2026-09-21 |
| FDA registration number | 3007923096 |
| Registration expires | 2027-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

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.