Dannik, LLC - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Dannik, LLC has 3 FDA 510(k) cleared medical devices. Based in Winter Park, US.
Latest FDA clearance: Mar 2025. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dannik, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Dannik, LLC
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