FDA Device Establishments · JSON-LD · Markdown
FEI 3000931034 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3000931034 |
|---|---|
| Owner / Operator | STRYKER CORP. (#1811755) |
| Address | 161 rue Lavoisier, Montbonnot Saint-Martin Isere, 38330, FR |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HXX |
| Regulation § (21 CFR) | 888.4540 |
| Proprietary names | ORTHOPEDIC SCREWDRIVER; STRYKER AUTOMATIC SCREWDRIVER; SET SCREWDRIVER; OSTEONICS; Cross-Screw System; Universal ACL Instrumentation; Biosteon Wedge Interference Screw System; ACL Reconstruction Accessories; Bioabsorable Wedge Interference Screw System; DRIVER; SCREW INSERTER |
Source: openFDA. Public-domain (CC0).