Boddingtons Plastics, Ltd. is one of 365 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Boddingtons Plastics, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Arc Enterocuff, Arc Endocuff Glide AEG110 & AEG120, Arc EndoCuff and Arc EndoCuff Vision
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.
510(k) submissions have been managed by Bsi Healthcare as regulatory consultant.
FDA 510(k) Regulatory Record - 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