# Zimmer India Private Limited (foreign exporter, Gurugram Haryana, IN): 3 new FDA device listings, incl. prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, 

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Zimmer India Private Limited |
| 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 | Gurugram Haryana, IN |
| New listings | 3 |
| Devices | Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
| Product codes | MBH, OIY, JWH |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | Persona Revision Knee System |
| First new listing | 2026-05-07 |
| Latest new listing | 2026-05-07 |
| FDA registration number | 3048147961 |
| Registration expires | 2026-12-31 |

## 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: 2026-10-28T20:51:27.468Z.
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.