Dannik, LLC - FDA 510(k) Cleared Devices
Recent clearances: DANNIK® Laparoscopic Single-Use Poly Specimen Retrieval System, Disposable Monopolar Laparoscopic Tips and Reusable Handles, Disposable Monopolar Laparoscopic Shafts and Reusable Handles
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dannik, LLC General & Plastic Surgery ✕
3 devices
Cleared
Mar 12, 2025
DANNIK® Laparoscopic Single-Use Poly Specimen Retrieval System
General & Plastic Surgery
27d
Cleared
Oct 28, 2021
Disposable Monopolar Laparoscopic Tips and Reusable Handles
General & Plastic Surgery
206d
Cleared
Aug 16, 2021
Disposable Monopolar Laparoscopic Shafts and Reusable Handles
General & Plastic Surgery
171d