Diros Technology, Inc. is one of 5582 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diros Technology, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Diros Technology, Inc. has 8 FDA 510(k) cleared medical devices. Based in Charleston, US.
Historical record: 8 cleared submissions from 2002 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Diros Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diros Technology, Inc.
8 devices
Cleared
Jun 27, 2017
OWL RF INSULATED CANNULAE
Neurology
111d
Cleared
Jul 30, 2015
Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and...
Neurology
167d
Cleared
Dec 30, 2014
OWL CANNULAE
Neurology
200d
Cleared
Jun 03, 2011
OWL CANNULAE
Neurology
269d
Cleared
May 05, 2011
OWL RF PROBES
Neurology
64d
Cleared
Jan 22, 2010
OWL UNIVERSAL RF SYSTEM URF-3AP (ML)
Neurology
105d
Cleared
Sep 27, 2006
OWL URF-3AP
Neurology
12d
Cleared
Jul 01, 2002
OWL RADIOFREQUENCY SYSTEM, MODEL URF-2AP
Neurology
25d