# Smith & Nephew, Inc. (manufacturer, Memphis, TN): 2 new FDA device listings, incl. prosthesis, knee, patellofemorotibial, semi-constrained, cemented, pol

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Smith & Nephew, Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Memphis, TN, US |
| New listings | 2 |
| Devices | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer |
| Product codes | JWH, MBH |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | LANDMARK Total Knee System |
| First new listing | 2026-09-14 |
| Latest new listing | 2026-09-14 |
| FDA registration number | 1020279 |
| 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.
- 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.