FDA Device Establishments · JSON-LD · Markdown
FEI 3006059917 · Remanufacture Medical Device · Status: Active
| FEI Number | 3006059917 |
|---|---|
| Owner / Operator | Stingray Surgical Products (#10026274) |
| Address | 1701 Costa Del Sol, Boca Raton, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HDF |
| Regulation § (21 CFR) | 884.4520 |
| Proprietary names | Stingray Leep/ Lletz Speculum |
Source: openFDA. Public-domain (CC0).