FDA Device Establishments · JSON-LD · Markdown
FEI 3010667733 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3010667733 |
|---|---|
| Owner / Operator | STRYKER CORP. (#1811755) |
| Address | 1023 Cherry Road, Memphis, TN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MQV |
| Regulation § (21 CFR) | 888.3045 |
| Proprietary names | PRO-DENSE |
Source: openFDA. Public-domain (CC0).