Artech Corp.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K911735 | ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT | DZE | 1992-03-05 | View |
| 510(k) | K895267 | ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT | DZE | 1990-04-10 | View |
| 510(k) | K891346 | ARTECH TYPE SS SUBMERGED SCREW IMPLANT | DZE | 1989-12-21 | View |
| 510(k) | K894160 | HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL | DZE | 1989-09-28 | View |
| 510(k) | K894151 | IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT | DZJ | 1989-09-27 | View |
| 510(k) | K894150 | COUNTERBORE FOR SS SUBMERGED SCREW PLANT | DZJ | 1989-09-27 | View |
| 510(k) | K843217 | HOLLOW BASKET DENTAL IMPLANTS | DZE | 1984-10-15 | View |
| 510(k) | K843218 | TPS SCREW DENTAL IMPLANTS | DZE | 1984-09-27 | View |
No matching devices.
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