ClearanceBrief
Company · US

Us Medical Innovations, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2011 to 2024. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEIElectrosurgical, Cutting & Coagulation & Accessories3
GCJLaparoscope, General & Plastic Surgery1
OABLow Energy Direct Current Thermal Ablation System1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 3, 2024K240297Canady Helios Cold Plasma™ XL-1000CP™ Ablation System (XL-1000CPSYS)
Us Medical Innovations, LLC
OAB
Nov 22, 2022K212736Canady Flex RoboWrist
Us Medical Innovations, LLC
GCJ
Nov 21, 2019K192124Canady Plasma SMART XL-1000 Electrosurgical Generator with Accessories
Us Medical Innovations, LLC
GEI
Dec 9, 2011K113500CANADY VIEIRA HYBRID PLASMA SCALPEL
Us Medical Innovations, LLC
GEI
Apr 6, 2011K100669CANADY PLASMA ELECTROSURGICAL UNIT SERIES WITH ACCESSORY PROBES AND BLADES
Us Medical Innovations, LLC
GEI

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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