# Tecomet Inc. (contract manufacturer, Wilmington, MA): 3 new FDA device listings, incl. prosthesis, hip, semi-constrained, metal/polymer, cemented

**Score:** 90/100

| Field | Value |
|---|---|
| Establishment | Tecomet Inc. |
| Owner / operator | Tecomet |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Wilmington, MA, US |
| New listings | 3 |
| Devices | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Product codes | JDI, JWH, LPH |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | Alpine Hip Stem; Offset Tibia Adapter; Encompass Hip Stem |
| First new listing | 2026-10-15 |
| Latest new listing | 2026-10-15 |
| FDA registration number | 1225675 |
| 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.
- U.S. establishment.
- Listed in the last 45 days.

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.