Cleared Traditional

K140293 - TOUAREG NP CLOSEFIT DENTAL IMPLANTS SYSTEM (FDA 510(k) Clearance)

Oct 2014
Decision
268d
Days
Class 2
Risk

K140293 is an FDA 510(k) clearance for the TOUAREG NP CLOSEFIT DENTAL IMPLANTS SYSTEM. This device is classified as a Implant, Endosseous, Root-form (Class II - Special Controls, product code DZE).

Submitted by Adin Dental Implants Systems , Ltd. (Pob 1128 Afula Elit, IL). The FDA issued a Cleared decision on October 31, 2014, 268 days after receiving the submission on February 5, 2014.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3640.

Submission Details

510(k) Number K140293 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 2014
Decision Date October 31, 2014
Days to Decision 268 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code DZE - Implant, Endosseous, Root-form
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.3640

Similar Devices - DZE Implant, Endosseous, Root-form

All 51
Adin Long Dental Implant System
K252031 · Adin Dental Implant Systems , Ltd. · Mar 2026
ZENEX Implant System_Short (R-System)
K253334 · Izenimplant Co., Ltd. · Mar 2026
Straumann® BLC Implants - Indication Widening
K252168 · Institut Straumann AG · Mar 2026
Dentis SQ-SL AXEL Fixture
K253493 · Dentis Co., Ltd. · Mar 2026
Nobel Biocare S Series Implants
K252197 · Nobel Biocare AB · Feb 2026
BIORES Dental Implant System
K252286 · Chengdu Besmile Medical Technology Co., Ltd. · Feb 2026