FDA 510(k) Applications Submitted by Ortek Therapeutics, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K002989 | 09/25/2000 | PROCLUDE | ORTEK THERAPEUTICS, INC. |
| K003482 | 11/09/2000 | PROCLUDE-SENSITIVE | ORTEK THERAPEUTICS, INC. |
| K170822 | 03/20/2017 | Electronic Caries Detector | Ortek Therapeutics, Inc. |
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