# Zimmer (Shanghai) Medical International Trading Co., Ltd. (foreign exporter, Shanghai, CN): 11 new FDA device listings, incl. prosthesis, knee, patellofemorotibial, semi-constrained, cemented, pol

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Zimmer (Shanghai) Medical International Trading Co., Ltd. |
| Owner / operator | Zimmer Biomet APAC DFE |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Shanghai, CN |
| New listings | 11 |
| Devices | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Plate, Fixation, Bone; Screw, Fixation, Bone; Cerclage, Fixation; Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented; Hip, Semi-Constrained, Cemented, Metal/Polymer + Additive, Cemented; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Product codes | JWH, HRS, HWC, JDQ, OQG, OQH, JDI, OQI, LZO, LPH |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | VANGUARD SSK 360 REVISION KNEE SYSTEM; Zimmer Periarticular Locking Plate System; Cable-Ready Cable Grip System; Cable-Ready Bone Plate System; G7 Acetabular System |
| First new listing | 2026-06-29 |
| Latest new listing | 2026-08-04 |
| FDA registration number | 3015207155 |
| Registration expires | 2027-12-31 |

## Why this score
- 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.