Gm Dos Reis Industria E Comerico Ltda.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest FDA decision2023-08-02
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K223114 | Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors | MBI | 2023-08-02 | View |
| 510(k) | K182718 | Mini and Micro Fragments Reconstruction System – GMReis | HRS | 2019-12-23 | View |
| 510(k) | K180626 | Pedimax II - Pedicular Screw Spinal System | NKB | 2019-02-01 | View |
No matching devices.