Laborie Medical Technologies, Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Laborie Medical Technologies, Corp. has 5 FDA 510(k) cleared medical devices. Based in Williston, US.
Latest FDA clearance: Aug 2024. Active since 2008. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Laborie Medical Technologies, Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Laborie Medical Technologies, Corp.
5 devices
Cleared
Aug 27, 2024
injeTAK Adjustable Tip Needle (DIS199
Gastroenterology & Urology
90d
Cleared
May 06, 2024
Solar Compact (G4-1)
Gastroenterology & Urology
125d
Cleared
Apr 23, 2024
Solar™ Anorectal Manometry Catheter (Model Number: K1210AC-L-2212)
Gastroenterology & Urology
119d
Cleared
Jul 09, 2008
NUWAV
Radiology
15d
Cleared
Mar 05, 2008
LABORIE URODYNAMIC SYSTEM WITH TETRA ACCESSORY
Gastroenterology & Urology
78d