FDA Device Establishments · JSON-LD · Markdown
FEI 3031288142 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 3031288142 |
|---|---|
| Owner / Operator | Gravity Medical Technology (#10090908) |
| Address | Suite E, 105 N Pointe Dr., Lake Forest, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | POL |
| Regulation § (21 CFR) | 882.5600 |
| Proprietary names | Supernova Revascularization Device |
Source: openFDA. Public-domain (CC0).