Acera Surgical, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories3
Latest Approval2025-06-20
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K251224 | Restrata Soft Tissue Reinforcement (STR) | OXF | 2025-06-20 | View |
| 510(k) | K223725 | Restrata® MiniMatrix | QSZ | 2023-05-18 | View |
| 510(k) | K193583 | Restrata® | QSZ | 2020-09-25 | View |
| 510(k) | K172603 | Cerafix Dura Substitute | GXQ | 2017-11-27 | View |
| 510(k) | K170300 | Restrata Wound Matrix | QSZ | 2017-04-26 | View |
| 510(k) | K161278 | Cerafix Dura Substitute | GXQ | 2016-08-08 | View |
| 510(k) | K153613 | Cerafix Dura Substitute | GXQ | 2016-03-16 | View |
No matching devices.