Xodus Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Xodus Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in New Kensington, US.
Latest FDA clearance: Apr 2026. Active since 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Xodus Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
6 devices
Cleared
Apr 16, 2026
Hot Pink Pad Warming System
Cardiovascular
29d
Cleared
Sep 19, 2018
Scope Antifogging System
General & Plastic Surgery
48d
Cleared
Aug 12, 2008
ELECTROSURGICAL PENCIL WITH PTFE COATED & UNCOATED ELECTRODE TIPS
General & Plastic Surgery
61d
Cleared
Jan 09, 2007
XODUS MEDICAL ANTI-FOG SOLUTION
Gastroenterology & Urology
39d
Cleared
Jan 19, 2006
LIGHT GUARD LIGHT HANDLE AND LIGHT HANDLE COVER
General & Plastic Surgery
50d
Cleared
Jan 19, 2006
CAUTERY TIP CLEANER, MODEL 30500
General & Plastic Surgery
41d