Medical Device Manufacturer · US , Los Angeles , CA

Dentecon, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991
2
Total
2
Cleared
0
Denied

Dentecon, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 2 cleared submissions from 1991 to 1994. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Dentecon, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dentecon, Inc.

2 devices
1-2 of 2
Cleared Nov 01, 1994
THERMABOND V
K926378 · EJT
Dental · 679d
Cleared May 30, 1991
THERMABOND SUPERCAST NP OR THERMABOND SUPERCAST
K911821 · EJH
Dental · 36d
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