Argon Medical Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Argon Medical Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ZeniCore™ Automatic Biopsy Instrument (863212100 / ZeniCore Automatic Biopsy Device 12ga x 10cm with Coaxial Introducer Kit), CLEANER™ Vac Thrombectomy System, CLEANER™ Vac Aspiration Catheter with Handpiece, CLEANER™ Vac Aspiration Canister, VariFuse Adjustable Infusion Catheter
Argon Medical Devices, Inc. manufactures specialty interventional medical devices. The company is based in Athens, US.
Argon has received 20 FDA 510(k) clearances from 20 total submissions since 2007. The company specializes in Cardiovascular devices, which represent the dominant focus of its regulatory portfolio. The latest clearance was in 2026, reflecting continued active development and market engagement.
Argon's cleared device portfolio includes thrombectomy systems, vascular access devices, biopsy instruments, and retrieval kits. The company also offers custom product solutions and maintains a comprehensive clinical education and training program for medical professionals.
Explore the complete list of device names, product codes, and clearance dates in the database.