Medical Device Manufacturer · US , Redwood City , CA

Laurimed, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2008
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
1-8 of 8
Cleared Mar 09, 2017
3.3 mm Laurimed Microdebrider
K163247 · ERL
Ear, Nose, Throat · 111d
Cleared Jun 22, 2016
PolypVac Microdebrider (3.3mm and 4.0mm)
K161101 · ERL
Ear, Nose, Throat · 64d
Cleared Dec 23, 2013
LAURIMED POLYPVAC MICRODEBRIDER
K133133 · ERL
Ear, Nose, Throat · 84d
Cleared Sep 23, 2009
LAURIMED SPINAL INJECTION SYSTEM
K091818 · BSP
Anesthesiology · 97d
Cleared May 21, 2009
PERCUTANEOUS DISCECTOMY SYSTEM
K090815 · HRX
Orthopedic · 57d
Cleared Mar 18, 2009
SPINAL INJECTION SYSTEM
K083909 · BSP
Anesthesiology · 78d
Cleared Aug 28, 2008
LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002
K082194 · HRX
Orthopedic · 24d
Cleared May 09, 2008
LAURIMED SPINAL INJECTION SYSTEM
K080140 · BSP
Anesthesiology · 108d
Filters
Filter by Specialty
All8 Ear, Nose, Throat 3 Anesthesiology 3 Orthopedic 2