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 |