Conmed Corporation - FDA 510(k) Cleared Devices

Conmed Corporation, is a global medical device manufacturer specializing in surgical equipment and operating room solutions. The company operates with a manufacturing facility in Utica, US, and serves multiple surgical specialties including general surgery, orthopedics, and patient monitoring.

Conmed has received 83 FDA 510(k) clearances from 83 total submissions since its first clearance in 2004. The company maintains active regulatory engagement, with its most recent clearance in 2026. Its cleared devices focus primarily on General & Plastic Surgery applications, including electrosurgical systems, vessel sealers, insufflation platforms, and surgical visualization technologies.

Recent cleared devices demonstrate Conmed's core competencies in advanced energy platforms, fluid management systems, and integrated surgical visualization. The company's product portfolio spans electrosurgical generators, bipolar resection systems, argon-based surgical tools, suction and irrigation systems, and tissue retrieval devices. These offerings support minimally invasive and open surgical procedures across multiple specialties.

Explore Conmed's complete FDA 510(k) clearance history, including specific device names, product codes, and clearance dates in the regulatory database.

Regulatory submissions have been managed by Daniel & Daniel Consulting, LLC and BioVera, Inc..