London Intl., LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
London Intl., LLC - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
London Intl., LLC has 6 FDA 510(k) cleared medical devices. Based in Dothan, US.
Historical record: 6 cleared submissions from 1998 to 1998. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by London Intl., LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - London Intl., LLC
6 devices
Cleared
Nov 16, 1998
DUREX SENSIDOM LATEX CONDOM
Obstetrics & Gynecology
88d
Cleared
Nov 16, 1998
DUREX LUBRAGEL LATEX CONDOM
Obstetrics & Gynecology
52d
Cleared
Aug 13, 1998
DUREX COLORS AND SCENTS
Obstetrics & Gynecology
205d
Cleared
Jun 10, 1998
STERILE, POWDERFREE LATEX EXAMINATION GLOVE
General Hospital
100d
Cleared
May 20, 1998
DUREX ULTRA COMFORT
Obstetrics & Gynecology
113d
Cleared
Apr 17, 1998
DUREX LATEX CONDOMS
Obstetrics & Gynecology
87d