Medical Device Manufacturer · IT , Peschiera Borromeo

Cedic S.R.L. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2005

Total

Cleared

Denied

Cedic S.R.L. has 7 FDA 510(k) cleared medical devices. Based in Peschiera Borromeo, IT.

Historical record: 7 cleared submissions from 2005 to 2019. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Cedic S.R.L. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Koelper Consulting, LLC and Donawa Lifescience Consulting Srl.

Cedic S.R.L. is one of 182 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cedic S.R.L.

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Jun 02, 2026