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
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
30d slower than avg
Panel avg: 128d · 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 Consultant

PaxMed International, LLC
LINDA SCHULZ

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - DZE Implant, Endosseous, Root-form

All 1370
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K151916.
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K150388 · Bio Concept Co., Ltd. · Nov 2015