Ortek Therapeutics, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K170822 | Electronic Caries Detector | NBL | 2017-09-11 | View |
| 510(k) | K003482 | PROCLUDE-SENSITIVE | LBH | 2001-02-01 | View |
| 510(k) | K002989 | PROCLUDE | EJR | 2000-12-14 | View |
No matching devices.
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