Medical Device Manufacturer · US , Los Angeles , CA

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

2 submissions · 2 cleared · Since 2010

Recent clearances: PHYSIOSTAR NFC, DIRECT CROWN NATURAL 1

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Candulor USA, Inc. Dental ✕

2 devices

1-2 of 2

Cleared Dec 06, 2012

Cleared Sep 27, 2010

DIRECT CROWN NATURAL 1

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 18, 2026