Hemedex Incorporated is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hemedex Incorporated - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Hemedex Incorporated has 4 FDA 510(k) cleared medical devices. Based in Hopkonton, US.
Historical record: 4 cleared submissions from 2002 to 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Hemedex Incorporated Filter by specialty or product code using the sidebar.
Hemedex Incorporated — FDA 510(k) Products and Clearance History
4 devices
Cleared
Oct 10, 2014
QFLOW 500 TITANIUM BOLT, QUAD LUMEN BOLT KIT
Neurology
91d
Cleared
Dec 30, 2003
HEMEDEX FIXATION DEVICE
Gastroenterology & Urology
173d
Cleared
Oct 21, 2003
HEMEDEX CRANIAL BOLT MODELS, 3601, 3602
Neurology
84d
Cleared
May 08, 2002
QFLOW 500 PERFUSION MONITORING SYSTEM
Cardiovascular
209d