Veran Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Veran Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SPiN Vision Video Bronchoscope System
7
Total
7
Cleared
0
Denied
Veran Medical Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Nashville, US.
Last cleared in 2021. Active since 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Veran Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Veran Medical Technologies, Inc.
7 devices
Cleared
Feb 19, 2021
SPiN Vision Video Bronchoscope System
Ear, Nose, Throat
185d
Cleared
May 15, 2017
SPiN Thoracic Navigation System
Radiology
132d
Cleared
Dec 21, 2012
SPIN DRIVE ALWAYS-ON TIP TRACKED STEERABLE CATHETER ALWAYS-ON TIP TRACKED...
Radiology
157d
Cleared
Jan 27, 2010
IG 4 IMAGE GUIDED SYSTEM
Radiology
30d
Cleared
Dec 02, 2009
IG4 ENDOBRONCHIAL, MODEL SYS-0200, NAVIGATION GUIDEWIRE (ACCESSORY TO IG4...
Radiology
155d
Cleared
Nov 30, 2009
IG4 IMAGE GUIDED SYSTEM, MODEL: SYS-0200
Radiology
56d
Cleared
May 11, 2006
IG4 IMAGE GUIDED SYSTEM
Radiology
38d