Gm Dos Reis Industria E Comerico Ltda.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K223114 | Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors | August 2, 2023 |
| K182718 | Mini and Micro Fragments Reconstruction System GMReis | December 23, 2019 |
| K180626 | Pedimax II - Pedicular Screw Spinal System | February 1, 2019 |