Gm Dos Reis Industria E Comerico Ltda. - FDA 510(k) Cleared Devices
Recent clearances: Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors, Mini and Micro Fragments Reconstruction System – GMReis, Pedimax II - Pedicular Screw Spinal System
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Gm Dos Reis Industria E Comerico Ltda. Orthopedic ✕
3 devices