ImpediMed Limited - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
ImpediMed Limited has 12 FDA 510(k) cleared gastroenterology & urology devices. Based in San Diego, US.
Latest FDA clearance: Jan 2026. Active since 2011.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by ImpediMed Limited
12 devices
Cleared
Jan 28, 2026
MySOZO Software version 6.0.1.2 (SW version 6.0.1.2)
Gastroenterology & Urology
121d
Cleared
Oct 17, 2023
SOZO Pro
Gastroenterology & Urology
96d
Cleared
May 04, 2023
SOZO Pro
Gastroenterology & Urology
66d
Cleared
May 04, 2023
SOZO Pro
Gastroenterology & Urology
66d
Cleared
Apr 19, 2021
SOZO
Gastroenterology & Urology
145d
Cleared
Oct 02, 2020
SOZO Body Fluid Analyzer
Gastroenterology & Urology
298d
Cleared
Nov 25, 2019
SOZO
Gastroenterology & Urology
266d
Cleared
Apr 16, 2018
SOZO
Gastroenterology & Urology
90d
Cleared
Dec 22, 2017
SOZO
Cardiovascular
126d
Cleared
Aug 11, 2017
SOZO
Gastroenterology & Urology
29d
Cleared
May 31, 2013
IMPEDIMED - BIS EXTRA CELLULAR FLUID ANALYSIS
Gastroenterology & Urology
109d
Cleared
Nov 04, 2011
IMPEDIMED - EXTRACELLULAR FLUID ANALYZER MODEL: L-DEX U400
Gastroenterology & Urology
592d