FDA Device Establishments · JSON-LD · Markdown
FEI 3003791208 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3003791208 |
|---|---|
| Owner / Operator | Tecomet (#1828464) |
| Address | 5212 Aurelius Rd, 5858 Enterprise Drive, Lansing, MI, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HWE |
| Regulation § (21 CFR) | 878.4820 |
| Proprietary names | Basket Reamer 40mm Hex; Patella Preparation; Superpath; Acetabular Reamer; Offset Reamer Driver; MBT Central Drill; Instrument, Surgical, Orthopedic, AC-Powered Motor and Accessory/Attachment |
Source: openFDA. Public-domain (CC0).