# Perryman Company (contract manufacturer, Houston, PA): 1 new FDA device listing, incl. prosthesis, knee, patellofemorotibial, semi-constrained, cemented, pol

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Perryman Company |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Houston, PA, US |
| New listings | 1 |
| Devices | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
| Product codes | JWH |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | ORT - CK Tibial Insert (563-1-1XXXX), Device Listing: D123579; ORT - Constrained Tibial Insert (563-1-2XXXX), Device Listing: D123575 |
| First new listing | 2026-07-08 |
| Latest new listing | 2026-07-08 |
| FDA registration number | 3009882462 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- 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.