Allmed Systems, Inc. is one of 5129 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allmed Systems, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Allmed Systems, Inc. has 8 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 8 cleared submissions from 2004 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Allmed Systems, Inc. Filter by specialty or product code using the sidebar.
Allmed Systems, Inc. — FDA 510(k) Products and Clearance History
8 devices
Cleared
Mar 18, 2014
SPHINX JR
General & Plastic Surgery
176d
Cleared
Feb 19, 2013
REVOLIX JR 30, REVOLIX JR 50, REVOLIX JR 160, REVOLIX FR 200
General & Plastic Surgery
687d
Cleared
Jun 21, 2007
FLEXGUARD
General & Plastic Surgery
79d
Cleared
Apr 17, 2007
REVOLIX DUO LASER SYSTEM
General & Plastic Surgery
60d
Cleared
Mar 26, 2007
REVOLIX 120
General & Plastic Surgery
34d
Cleared
Jun 01, 2005
REVOLIX AND REVOLIX JR
General & Plastic Surgery
27d
Cleared
Jan 20, 2004
SPHINX LASER SYSTEMS
General & Plastic Surgery
84d
Cleared
Jan 15, 2004
REVOLIX LASER SYSTEMS
General & Plastic Surgery
80d