Helios Biomedical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2025-08-15
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250397 | Helios Dermal Scaffold | KGN | 2025-08-15 | View |
| 510(k) | K250420 | Helios Dura Regeneration Matrix | GXQ | 2025-05-14 | View |
No matching devices.