FDA Device Establishments · JSON-LD · Markdown
FEI 3041915827 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 3041915827 |
|---|---|
| Owner / Operator | NovaTech Scientific (#10094103) |
| Address | 399 Nw 2nd Ave Ste 216, Boca Raton, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HRX |
| Regulation § (21 CFR) | 888.1100 |
| Proprietary names | NovaTech Percutaneous Discectomy Kit; BIDISK KIT 17G; BiDisk Percutaneous Discectomy Kit |
Source: openFDA. Public-domain (CC0).