Medical Device Manufacturer · US , New York , NY

Ortek Therapeutics, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2000

Total

Cleared

Denied

Ortek Therapeutics, Inc. has 3 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 3 cleared submissions from 2000 to 2017. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Ortek Therapeutics, Inc.

3 devices

1-3 of 3