FDA Device Establishments · JSON-LD · Markdown
FEI 3008395366 · Export Device to the United States But Perform No Other Operation on Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3008395366 |
|---|---|
| Owner / Operator | Osteotec Limited (#10032513) |
| Address | Building 81, Greenham Business Park, Newbury West Berkshire, RG19 6HW, GB |
| Mandatory US Agent | TriMed Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HTQ |
| Regulation § (21 CFR) | 888.4540 |
| Proprietary names | Osteotec Silicone Finger Rasp |
Source: openFDA. Public-domain (CC0).