Boddingtons Plastics, Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Boddingtons Plastics, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Tonbridge, Kent, GB.
Historical record: 5 cleared submissions from 2012 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Boddingtons Plastics, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Boddingtons Plastics, Ltd.
5 devices
Cleared
Jan 31, 2020
Arc Enterocuff
Gastroenterology & Urology
260d
Cleared
May 30, 2019
Arc Endocuff Glide AEG110 & AEG120
Gastroenterology & Urology
38d
Cleared
Dec 09, 2016
Arc EndoCuff and Arc EndoCuff Vision
Gastroenterology & Urology
126d
Cleared
Aug 13, 2015
Arc Endocuff Vision
Gastroenterology & Urology
42d
Cleared
Sep 04, 2012
ARC ENDOCUFF
Gastroenterology & Urology
13d