Dyonics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM, DYONICS SHOULDER PORTAL SYSTEM, SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTY
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dyonics, Inc. General & Plastic Surgery ✕
2 devices