Medical Device Manufacturer · US , Santa Fe Springs , CA

Dio Department Dsi, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2006

Recent clearances: SECURE IMPLANT SYSTEM (2.5/3.0MM), DIO BIOTITE-H IMPLANT SYSTEM, SM-EXTRA WIDE (RBM) IMPLANT SYSTEM

View 8 510(k) Devices ↓
8
Total
8
Cleared
0
Denied

FDA 510(k) Regulatory Record - Dio Department Dsi, Inc. Dental ✕

8 devices
1-8 of 8
Cleared May 30, 2008
SECURE IMPLANT SYSTEM (2.5/3.0MM)
K080129 · DZE
Dental · 134d
Cleared May 16, 2008
DIO BIOTITE-H IMPLANT SYSTEM
K073070 · DZE
Dental · 199d
Cleared May 14, 2008
SM-EXTRA WIDE (RBM) IMPLANT SYSTEM
K080128 · DZE
Dental · 118d
Cleared Apr 15, 2008
DIO IMPLANT SYSTEM
K070570 · DZE
Dental · 412d
Cleared Apr 11, 2008
DIO PROTEM IMPLANT SYSTEM
K080126 · DZE
Dental · 85d
Cleared Nov 08, 2007
SM INTERNAL./EXTERNAL IMPLANT SYSTEM
K070569 · DZE
Dental · 253d
Cleared May 25, 2007
DIO PROTEM IMPLANT SYSTEM
K070568 · DZE
Dental · 86d
Cleared Sep 01, 2006
SM IMPLANT SYSTEMS
K061797 · DZE
Dental · 67d
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