Laurimed, LLC is one of 15069 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laurimed, LLC - FDA 510(k) Cleared Devices
Recent clearances: 3.3 mm Laurimed Microdebrider, PolypVac Microdebrider (3.3mm and 4.0mm), LAURIMED POLYPVAC MICRODEBRIDER
8
Total
8
Cleared
0
Denied
Laurimed, LLC has 8 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 8 cleared submissions from 2008 to 2017.
Browse the FDA 510(k) cleared devices submitted by Laurimed, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laurimed, LLC
8 devices
Cleared
Mar 09, 2017
3.3 mm Laurimed Microdebrider
Ear, Nose, Throat
111d
Cleared
Jun 22, 2016
PolypVac Microdebrider (3.3mm and 4.0mm)
Ear, Nose, Throat
64d
Cleared
Dec 23, 2013
LAURIMED POLYPVAC MICRODEBRIDER
Ear, Nose, Throat
84d
Cleared
Sep 23, 2009
LAURIMED SPINAL INJECTION SYSTEM
Anesthesiology
97d
Cleared
May 21, 2009
PERCUTANEOUS DISCECTOMY SYSTEM
Orthopedic
57d
Cleared
Mar 18, 2009
SPINAL INJECTION SYSTEM
Anesthesiology
78d
Cleared
Aug 28, 2008
LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002
Orthopedic
24d
Cleared
May 09, 2008
LAURIMED SPINAL INJECTION SYSTEM
Anesthesiology
108d