Alveolus, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alveolus, Inc. - FDA 510(k) Cleared Devices
12
Total
7
Cleared
0
Denied
Alveolus, Inc. has 7 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Historical record: 7 cleared submissions from 2003 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Alveolus, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alveolus, Inc.
12 devices
Cleared
Mar 11, 2009
AERO DV TRACHEOBRONCHIAL STENT SYSTEM
General & Plastic Surgery
93d
Cleared
Nov 20, 2008
AERO TRACHEOBRONCHIAL STENT TECHNOLOGY SYSTEM
General & Plastic Surgery
101d
Cleared
Apr 24, 2008
ALVEOLUS ALIMAXX-E ESOPHAGEAL STENT SYSTEM
Gastroenterology & Urology
30d
Cleared
Apr 11, 2008
ALIMAXX-B UNCOVERED BILIARY STENT SYSTEM
Gastroenterology & Urology
199d
Cleared
Sep 19, 2007
ALVEOLUS AERO DV TRACHEOBRONCHIAL STENT SYSTEM
General & Plastic Surgery
99d
Cleared
Jan 31, 2007
AERO TRACHEOBRONCHIAL STENT SYSTEM, MODEL 90129-2XX
General & Plastic Surgery
156d
Cleared
Mar 22, 2006
ALEOLUS/ENOVENTIONS,ALIMAXX-E DV ESOPHAGEAL STENT SYSTEM
Gastroenterology & Urology
50d
Cleared
Jul 11, 2005
ENDOVENTIONS ALIMAXX-E ESOPHAGEAL STENT SYSTEM
Gastroenterology & Urology
21d
Cleared
May 12, 2004
ALVEOLUS INC. TB-STS TRACHEOBRONCHIAL STENT SYSTEM
General & Plastic Surgery
141d
Cleared
Feb 25, 2004
ALVEOLUS, TB-STS TRACHEOBRONCHIAL STENT SYSTEM
General & Plastic Surgery
149d
Cleared
Nov 13, 2003
ALVEOLUS INC., TB-STS TRACHEOBRONCHIAL STENT SYSTEM
General & Plastic Surgery
70d
Cleared
May 15, 2003
ALVEOLUS INC., TB-STS TRACHEOBRONCHIAL STENT SYSTEM
General & Plastic Surgery
50d