Medical Device Manufacturer · US , Los Angeles , CA

Candulor USA, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied

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

Historical record: 2 cleared submissions from 2010 to 2012. Primary specialty: Dental.

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

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