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Sign in to claim this brandAcera Surgical Inc
US
Last updated May 23, 2026
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 040631370
Catalogue (35)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cerafix® Dura Substitute | C1-1X3 | FDA UDI | Class II | Active |
| Restrata Meshed | RMESH-4X5 | FDA UDI | U | Active |
| Restrata MiniMatrix | RMINI-1000 | FDA UDI | U | Active |
| Restrata Meshed | RMESH-2X2 | FDA UDI | U | Active |
| Cerafix® Dura Substitute | C1-4X5 | FDA UDI | Class II | Active |
| Cerafix® Dura Substitute | C1-1X1 | FDA UDI | Class II | Active |
| Restrata™ Wound Matrix | RWM1-1X3 | FDA UDI | U | Active |
| Restrata Meshed | RMESH-5X7 | FDA UDI | U | Active |
| Restrata(R) | RWM1-1X2 | FDA UDI | U | Active |
| Restrata™ Wound Matrix | RWM1-2X2 | FDA UDI | U | Active |
| Cerafix® Dura Substitute | C1-2X2 | FDA UDI | Class II | Active |
| Restrata MiniMatrix | RMINI-2000 | FDA UDI | U | Active |
| Restrata™ Wound Matrix | RWM1-1X1 | FDA UDI | U | Active |
| Restrata Wound Matrix | RWM1-5X7 | FDA UDI | U | Active |
| Restrata Wound Matrix | RWM1-0.5X1 | FDA UDI | U | Active |
| Restrata MiniMatrix | RMINI-500 | FDA UDI | U | Active |
| Restrata MiniMatrix | RMINI-100 | FDA UDI | U | Active |
| CovoraTM | COV1-7.5X7.5 | FDA UDI | U | Active |
| Cerafix® Dura Substitute | C1-3X3 | FDA UDI | Class II | Active |
| Restrata MiniMatrix | RMINI-250 | FDA UDI | U | Active |
| Restrata Wound Matrix | RWM1-1.5X2 | FDA UDI | U | Active |
| Cerafix® Dura Substitute | C1-5X7 | FDA UDI | Class II | Active |
| Restrata Meshed | RMESH-1.5X2 | FDA UDI | U | Active |
| Restrata™ Wound Matrix | RWM1-4X5 | FDA UDI | U | Active |
| Restrata Meshed | RMESH-3X3 | FDA UDI | U | Active |
| Restrata™ Wound Matrix | RWM1-3X3 | FDA UDI | U | Active |
| CovoraTM | COV1-10X12.5 | FDA UDI | U | Active |
| CovoraTM | COV1-5X5 | FDA UDI | U | Active |
| Restrata Soft Tissue Reinforcement (STR) | K251224 | FDA 510(k) | Class II | Active |
| Cerafix Dura Substitute | K153613 | FDA 510(k) | Class II | Active |
| Restrata® | K193583 | FDA 510(k) | U | Active |
| Cerafix Dura Substitute | K172603 | FDA 510(k) | Class II | Active |
| Cerafix Dura Substitute | K161278 | FDA 510(k) | Class II | Active |
| Restrata Wound Matrix | K170300 | FDA 510(k) | U | Active |
| Restrata® MiniMatrix | K223725 | FDA 510(k) | U | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 21, 2022 | Z-1030-2022 | — | terminated | Misprinted expiration date on the shelf-box |