Bioinfera, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K061323 | MODIFICATION TO RELIADENT DENTAL IMPLANT SYSTEM | DZE | 2007-05-23 | View |
| 510(k) | K043428 | RELIADENT DENTAL IMPLANT SYSTEM | NHA | 2005-07-12 | View |
No matching devices.
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