Smith & Nephew Dyonics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LIMITED REUSE ARTHROSCOPIC BLADES, ECTRA II LIGAMENT RELEASE SYSTEM, DYONICS DISPOSABLE ENDOSCOPIC SURGERY BLADES
22
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Smith & Nephew Dyonics, Inc. General Hospital ✕
1 devices