Medical Device Manufacturer · GB , Tonbridge, Kent

Boddingtons Plastics, Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2012

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
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