Broncus Medical, Inc. is one of 16567 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Broncus Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LungPoint Virtual Bronchoscopic Navigation (VBN) Software, BroncTru™ Transbronchial Access Tool, BioStar Single Use Transbronchial Aspiration Needle
7
Total
7
Cleared
0
Denied
Broncus Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Latest FDA clearance: Apr 2026. Active since 2013.
Browse the FDA 510(k) cleared devices submitted by Broncus Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Broncus Medical, Inc.
7 devices
Cleared
Apr 24, 2026
LungPoint Virtual Bronchoscopic Navigation (VBN) Software
Radiology
112d
Cleared
May 31, 2024
BroncTru™ Transbronchial Access Tool
Anesthesiology
277d
Cleared
Apr 26, 2024
BioStar Single Use Transbronchial Aspiration Needle
Anesthesiology
291d
Cleared
Jan 14, 2021
EasyPath RF Introducer Sheath
Ear, Nose, Throat
302d
Cleared
Feb 22, 2019
Empower RF Catheter
General & Plastic Surgery
94d
Cleared
Feb 26, 2014
LUNGPOINT ATV PLANNING AND NAVIGATION SOFTWARE
Radiology
113d
Cleared
Oct 15, 2013
LUNGPOINT TOOLS (LUNGPOINT SHEATH, LUNGPOINT DILATION BALLOON)
Ear, Nose, Throat
167d