FDA Device Establishments · JSON-LD · Markdown
FEI 1000132435 · Reprocess Single-Use Device · Status: Active
| FEI Number | 1000132435 |
|---|---|
| Owner / Operator | STRYKER CORP. (#1811755) |
| Address | 5307 Great Oak Drive, LAKELAND, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NLQ |
| Proprietary names | Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology |
Source: openFDA. Public-domain (CC0).