Laborie Medical Technologies, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laborie Medical Technologies, Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Laborie Medical Technologies, Ltd. has 11 FDA 510(k) cleared gastroenterology & urology devices. Based in North Attleboro, US.
Historical record: 11 cleared submissions from 1992 to 2009.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laborie Medical Technologies, Ltd.
11 devices
Cleared
Jul 21, 2009
LABORIE INJETAK ADJUSTABLE TIP NEEDLE, FLEXIBLE TIP AND RIDGID TIP
Gastroenterology & Urology
117d
Cleared
May 20, 1997
UROSTYM
Gastroenterology & Urology
363d
Cleared
Feb 16, 1996
TEX-AID BLUE
Gastroenterology & Urology
52d
Cleared
Jan 24, 1996
U-TEX
Gastroenterology & Urology
29d
Cleared
Jul 06, 1995
PIPER, MODEL NUMBER UDS-PIPERB
Gastroenterology & Urology
79d
Cleared
Jun 06, 1995
ELITE BIOFEEDBACK
Gastroenterology & Urology
371d
Cleared
Jul 12, 1994
INFUSION PUMP, MODEL NO. UDP-5
Gastroenterology & Urology
77d
Cleared
Nov 24, 1993
DRI SLEEPER
Gastroenterology & Urology
78d
Cleared
Aug 05, 1993
ADVANCE MODEL UDS-ADV
Gastroenterology & Urology
128d
Cleared
Mar 03, 1993
DRITRAINER
Gastroenterology & Urology
58d
Cleared
Oct 20, 1992
NICKI, MODEL NUMBER USD-NK-UP1
Gastroenterology & Urology
68d