Sientra, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2023-06-08
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K214124 | AlloX2 Pro Tissue Expanders | LCJ | 2023-06-08 | View |
| 510(k) | K221127 | Sientra, inc. Portfinder | LCJ | 2023-05-10 | View |
| 510(k) | K200706 | Sientra OPUS Silicone Gel Breast Implant Sizer | MRD | 2020-11-16 | View |
No matching devices.