Megagen Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Megagen Co., Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Megagen Co., Ltd. has 9 FDA 510(k) cleared medical devices. Based in Santa Fe Springs, US.
Historical record: 9 cleared submissions from 2005 to 2011. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Megagen Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Megagen Co., Ltd.
9 devices
Cleared
Nov 22, 2011
ANYRIDGE INTERNAL IMPLANT SYSTEM
Dental
231d
Cleared
Feb 03, 2011
BALL ABUTMENT SYSTEM
Dental
211d
Cleared
Apr 11, 2008
RESCUE INTERNAL IMPLANT SYSTEM
Dental
164d
Cleared
May 18, 2007
EZ PLUS IMPLANT SYSTEM
Dental
80d
Cleared
Apr 02, 2007
RESCUE INTERNAL IMPLANT SYSTEM
Dental
160d
Cleared
Apr 19, 2006
RESCUE IMPLANT SYSTEM
Dental
138d
Cleared
Apr 13, 2006
INTERMEZZO PLUS FIXTURE
Dental
132d
Cleared
Jan 10, 2006
EXFEEL IMPLANT SYSTEM
Dental
134d
Cleared
Sep 02, 2005
INTERMEZZO IMPLANT SYSTEMS
Dental
134d