Syntex Dental Products, 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) | K832378 | VIBRATORY ENDODONTIC SYSTEM | EKQ | 1983-10-04 | View |
| 510(k) | K823230 | STERILE WATER SYSTEM | EIA | 1982-12-03 | View |
| 510(k) | K822610 | PRECAPSULED DENTAL AMALGAM | DZS | 1982-09-14 | View |
No matching devices.
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