Lxn Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lxn Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Lxn Corp. has 7 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 7 cleared submissions from 1996 to 2001. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Lxn Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lxn Corp.
7 devices
Cleared
Feb 01, 2001
PERSONAL GLUCOSE CONTROL CHARTING SYSTEM
Chemistry
156d
Cleared
Sep 08, 1999
GO GLUCOSE MONITORING SYSTEM
Chemistry
107d
Cleared
Aug 02, 1999
DUET II GLUCOSE CONTROL MONITORING SYSTEM
Chemistry
133d
Cleared
Oct 31, 1997
DUET GLUCOSE CONTROL MONITORING SYSTEM
Chemistry
71d
Cleared
Jun 13, 1997
LXN FRUCTOSAMINE TEST SYSTEM
Chemistry
346d
Cleared
Jun 28, 1996
LXN BLOOD GLUCOSE TEST SYSTEM
Chemistry
177d
Cleared
Mar 20, 1996
LXN FRUCTOSAMINE TEST
Chemistry
100d