London International U.S. Holdings, Inc. is one of 14267 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
London International U.S. Holdings, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS, DUREX, RAMSES, SHEIK
2
Total
2
Cleared
0
Denied
London International U.S. Holdings, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sarasota, US.
Historical record: 2 cleared submissions from 1996 to 1996. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by London International U.S. Holdings, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - London International U.S. Holdings, Inc.
2 devices