Ortek Therapeutics, Inc. is one of 18594 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ortek Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Electronic Caries Detector, PROCLUDE-SENSITIVE, PROCLUDE
3
Total
3
Cleared
0
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.
510(k) submissions have been managed by Acknowledge Regulatory Strategies as regulatory consultant.
FDA 510(k) Regulatory Record - Ortek Therapeutics, Inc.
3 devices