Bioform Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO GFX NERVE ABLATION SYSTEM, RADIESSE LARYNGEAL IMPLANT, JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bioform Medical, Inc. Ear, Nose, Throat ✕
2 devices