Cleared Traditional

K151916 - TRI Dental Implant System

K151916 is an FDA 510(k) clearance for TRI Dental Implant System, manufactured by Tri Dental Implants Int. AG. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 158-day FDA review.

K151916 · Tri Dental Implants Int. AG · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2015
Decision
158d
Days
Class 2
Risk

K151916 is an FDA 510(k) clearance for the TRI Dental Implant System. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Tri Dental Implants Int. AG (Baar, CH). The FDA issued a Cleared decision on December 18, 2015 after a review of 158 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3640 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Tri Dental Implants Int. AG devices

FDA 510(k) Submission Details - K151916

510(k) Number K151916 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 2015
Decision Date December 18, 2015
Days to Decision 158 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
31d slower than avg
Panel avg: 127d · This submission: 158d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DZE Device Classification - Class 2, Special Controls

Product Code DZE Implant, Endosseous, Root-form
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3640
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - DZE Implant, Endosseous, Root-form

All 759
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K151916.
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Straumann® Dental Implant System ¿ Roxolid® SLA Implants
K150938 · Straumann USA, LLC · Jul 2015