London International Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
London International Group, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
London International Group, Inc. has 5 FDA 510(k) cleared medical devices. Based in Dotham, US.
Historical record: 5 cleared submissions from 1997 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by London International Group, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - London International Group, Inc.
5 devices
Cleared
Apr 12, 2000
REGENT SKINDENDE EXAM GLOVE, REGENT BIOGEL D, REGENTBIOGEL DIAGNOSTIC...
General Hospital
331d
Cleared
May 04, 1999
SKINSENSE NITRILE POWDER-FREE SYNTHETIC MEDICAL EXAMINATION GLOVE
General Hospital
155d
Cleared
May 11, 1998
REGENT BIOGEL INDICATOR INNER SURGICAL GLOVE
General Hospital
60d
Cleared
Apr 23, 1998
REGENT BIOGEL ORTHOPEDIC SURGICAL GLOVE
General Hospital
72d
Cleared
Oct 29, 1997
REGENT BIOGEL DIAGNOSTIC PROCEDURE GLOVE
General Hospital
187d