The following data is part of a premarket notification filed by Zest Anchors, Inc. with the FDA for Zest Implant Anchor Advanced Generation (dental).
| Device ID | K934668 |
| 510k Number | K934668 |
| Device Name: | ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL) |
| Classification | Implant, Endosseous, Root-form |
| Applicant | ZEST ANCHORS, INC. 2061 WINERIDGE PL., SUITE 100 Escondido, CA 92029 |
| Contact | Paul Zuest |
| Correspondent | Paul Zuest ZEST ANCHORS, INC. 2061 WINERIDGE PL., SUITE 100 Escondido, CA 92029 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-09-29 |
| Decision Date | 1994-06-22 |