Apyx Medical Corporation (Formerly Bovie Medical Corporation
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) | K220970 | Renuvion APR Handpiece | GEI | 2022-07-15 | View |
| 510(k) | K211652 | Renuvion Dermal Handpiece, Renuvion Dermal System | GEI | 2022-05-25 | View |
| 510(k) | K202880 | J-Plasma Precise FLEX Handpiece | GEI | 2021-01-04 | View |
| 510(k) | K191484 | Renuvion/J-Plasma Precise Handpiece | GEI | 2019-07-30 | View |
No matching devices.
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