Cleared Traditional

K151965 - Dentti System

K151965 is an FDA 510(k) clearance for Dentti System, manufactured by Martz, Inc.. The device is a Class 2 Dental device with product code NXC cleared through the Traditional 510(k) pathway after a 239-day FDA review.

K151965 · Martz, Inc. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 2016
Decision
239d
Days
Class 2
Risk

K151965 is an FDA 510(k) clearance for the Dentti System. Classified as Aligner, Sequential (product code NXC), Class II - Special Controls.

Submitted by Martz, Inc. (Bakersfield, US). The FDA issued a Cleared decision on March 11, 2016 after a review of 239 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.5470 - 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.

FDA 510(k) Submission Details - K151965

510(k) Number K151965 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 16, 2015
Decision Date March 11, 2016
Days to Decision 239 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
111d slower than avg
Panel avg: 128d · This submission: 239d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NXC Device Classification - Class 2, Special Controls

Product Code NXC Aligner, Sequential
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.5470
Definition The Device Moves The Teeth By Continuous Gentle Force For Treatment Of Minor Tooth Malocclusion.
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

Texel Fortis, LLC
Mason Diamond

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 - NXC Aligner, Sequential

All 144
Devices cleared under the same product code (NXC) and FDA review panel - the closest regulatory comparables to K151965.
ClearPath Aligner
K162609 · Clearpath Orthodontics, Ltd. · Jul 2017
MTM Clear Aligner
K163155 · Dentsply Sirona · Feb 2017
3M Clear Tray Aligner
K163689 · 3M Unitek Corporation · Jan 2017
Invisalign System
K143630 · Align Technology, Inc. · Nov 2015
eCligner
K143499 · Eclear International Co., Ltd. · Oct 2015
CLEARPATH ALIGNER
K123514 · Qserve America, Inc. · Nov 2013