Regenesis Biomedical, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K223620 | Reprieve by RegenesisTM | IMJ | 2023-05-24 | View |
| 510(k) | K131979 | PROVANT THERAPY SYSTEM | ILX | 2013-12-13 | View |
| 510(k) | K091791 | PROVANT SYSTEM, MODEL 4201 | ILX | 2010-04-07 | View |
| 510(k) | K972093 | REGENESIS MODEL 42 | ILX | 1997-10-21 | View |
No matching devices.
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