Us Medical Innovations, LLC - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Us Medical Innovations, LLC has 5 FDA 510(k) cleared medical devices. Based in Austin, US.
Latest FDA clearance: May 2024. Active since 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Us Medical Innovations, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Us Medical Innovations, LLC
5 devices
Cleared
May 03, 2024
Canady Helios Cold Plasma™ XL-1000CP™ Ablation System (XL-1000CPSYS)
General & Plastic Surgery
92d
Cleared
Nov 22, 2022
Canady Flex RoboWrist
General & Plastic Surgery
449d
Cleared
Nov 21, 2019
Canady Plasma SMART XL-1000 Electrosurgical Generator with Accessories
General & Plastic Surgery
107d
Cleared
Dec 09, 2011
CANADY VIEIRA HYBRID PLASMA SCALPEL
General & Plastic Surgery
14d
Cleared
Apr 06, 2011
CANADY PLASMA ELECTROSURGICAL UNIT SERIES WITH ACCESSORY PROBES AND BLADES
General & Plastic Surgery
393d