The following data is part of a premarket notification filed by Dentin Implants Technologies Ltd. with the FDA for Dentin Dental Implants System: Rapid, Classic, Prestige, One Piece, Dentin Dental Abutment System / Dentin Restoration S.
| Device ID | K120530 |
| 510k Number | K120530 |
| Device Name: | DENTIN DENTAL IMPLANTS SYSTEM: RAPID, CLASSIC, PRESTIGE, ONE PIECE, DENTIN DENTAL ABUTMENT SYSTEM / DENTIN RESTORATION S |
| Classification | Implant, Endosseous, Root-form |
| Applicant | DENTIN IMPLANTS TECHNOLOGIES LTD. 22817 VENTURA BLVD. #161 Woodland Hills, CA 91364 |
| Contact | Daniela Levy |
| Correspondent | Daniela Levy DENTIN IMPLANTS TECHNOLOGIES LTD. 22817 VENTURA BLVD. #161 Woodland Hills, CA 91364 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-02-22 |
| Decision Date | 2012-07-05 |
| Summary: | summary |