FDA Device Establishments · JSON-LD · Markdown
FEI 3016573902 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3016573902 |
|---|---|
| Owner / Operator | STRYKER CORP. (#1811755) |
| Address | 7 Halamish St, Caesarea Haifa, 3079579, IL |
| Mandatory US Agent | Stryker Endoscopy |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QPQ |
| Regulation § (21 CFR) | 888.3630 |
| Proprietary names | InSpace US Medium; InSpace US Small; InSpace US Large |
Source: openFDA. Public-domain (CC0).