Medical Device Manufacturer · US , Santa Fe Springs , CA

Megagen Co., Ltd. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2005

Recent clearances: ANYRIDGE INTERNAL IMPLANT SYSTEM, BALL ABUTMENT SYSTEM, RESCUE INTERNAL IMPLANT SYSTEM

View 9 510(k) Devices ↓
9
Total
9
Cleared
0
Denied

FDA 510(k) Regulatory Record - Megagen Co., Ltd. Dental ✕

9 devices
1-9 of 9
Cleared Nov 22, 2011
ANYRIDGE INTERNAL IMPLANT SYSTEM
K110955 · DZE
Dental · 231d
Cleared Feb 03, 2011
BALL ABUTMENT SYSTEM
K101890 · NHA
Dental · 211d
Cleared Apr 11, 2008
RESCUE INTERNAL IMPLANT SYSTEM
K073058 · DZE
Dental · 164d
Cleared May 18, 2007
EZ PLUS IMPLANT SYSTEM
K070562 · NHA
Dental · 80d
Cleared Apr 02, 2007
RESCUE INTERNAL IMPLANT SYSTEM
K063216 · DZE
Dental · 160d
Cleared Apr 19, 2006
RESCUE IMPLANT SYSTEM
K053353 · DZE
Dental · 138d
Cleared Apr 13, 2006
INTERMEZZO PLUS FIXTURE
K053354 · DZE
Dental · 132d
Cleared Jan 10, 2006
EXFEEL IMPLANT SYSTEM
K052369 · DZE
Dental · 134d
Cleared Sep 02, 2005
INTERMEZZO IMPLANT SYSTEMS
K051018 · DZE
Dental · 134d
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