FDA Device Establishments · JSON-LD · Markdown
FEI 3020745236 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3020745236 |
|---|---|
| Owner / Operator | Lincotek Medical, LLC (#9057128) |
| Address | 221 Commercial Parkway, Molalla, OR, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | HSD, KWT |
| Regulation § (21 CFR) | 888.3690, 888.3650 |
| Proprietary names | Catalyst CSR Press-Fit Humeral Component |
Source: openFDA. Public-domain (CC0).