# Depuy Orthopaedics, Inc. (manufacturer, Warsaw, IN): 12 new FDA device listings, incl. prosthesis, shoulder, semi-constrained, metal/polymer cemented

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Depuy Orthopaedics, Inc. |
| Owner / operator | DePuy Synthes, Inc. |
| Role | Manufacturer |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device |
| Location | Warsaw, IN, US |
| New listings | 12 |
| Devices | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented; Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented; Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented; Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented; Shoulder Prosthesis, Reverse Configuration; Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Orthopedic Stereotaxic Instrument; Bone Cement; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented |
| Product codes | KWS, MBF, HSD, KWT, PHX, MBH, JWH, OLO, LOD, KWY, MBB, KWL |
| Device classes | Class II |
| Medical specialties | Orthopedic, Neurology |
| First new listing | 2026-06-15 |
| Latest new listing | 2026-08-07 |
| FDA registration number | 1818910 |
| 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.

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.