GBUK Group, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
GBUK Group, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Enteral Transition Adaptor, Enteral Extension Sets
2
Total
2
Cleared
0
Denied
GBUK Group, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Selby, GB.
Last cleared in 2022. Active since 2021. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by GBUK Group, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - GBUK Group, Ltd.
2 devices