Conmed Corporation - FDA 510(k) Cleared Devices
82
Total
82
Cleared
0
Denied
Conmed Corporation has 82 FDA 510(k) cleared medical devices. Based in Utica, US.
Latest FDA clearance: Jan 2026. Active since 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Conmed Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Conmed Corporation
82 devices
Cleared
Jan 29, 2026
Y-Knotless™ Flex Anchors
Orthopedic
65d
Cleared
Oct 15, 2025
BioBrace® Extra-Articular Ligament Augmentation Kit
Orthopedic
30d
Cleared
Jun 18, 2025
CONMED Argo Knotless® Anchor
Orthopedic
30d
Cleared
Apr 07, 2025
BioBrace ® RC Delivery System
Orthopedic
54d
Cleared
Jan 28, 2025
Argo Knotless GENESYS Anchor
Orthopedic
32d
Cleared
Nov 27, 2024
BioBrace®
Orthopedic
125d
Cleared
Aug 05, 2024
PlumeSafe X5 Smoke Management System
General Hospital
201d
Cleared
Jul 29, 2024
BioBrace® Reinforced Implant
Orthopedic
28d
Cleared
Mar 05, 2024
Argo Knotless GENESYS Anchor
Orthopedic
53d
Cleared
Oct 23, 2023
CleanSeal Advanced Bipolar Vessel Sealer Maryland
General & Plastic Surgery
132d
Cleared
Sep 20, 2023
AirSeal iFS System
Obstetrics & Gynecology
233d
Cleared
Apr 27, 2023
PlumePen Elite Surgical Smoke Evacuation Pencils, PlumePen Pro Surgical Smoke...
General Hospital
58d
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