ImpediMed Limited - FDA 510(k) Cleared Devices

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.

Regulatory submissions have been managed by Impedimed, Inc. and Imedimed, Inc..