Cleared Traditional

K151909 - Noris Medical Zygomatic Dental Implant System

K151909 is an FDA 510(k) clearance for Noris Medical Zygomatic Dental Implant ..., manufactured by Noris Medical , Ltd.. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 270-day FDA review.

K151909 · Noris Medical , Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2016
Decision
270d
Days
Class 2
Risk

K151909 is an FDA 510(k) clearance for the Noris Medical Zygomatic Dental Implant System. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Noris Medical , Ltd. (Nesher, IL). The FDA issued a Cleared decision on April 8, 2016 after a review of 270 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 Noris Medical , Ltd. devices

FDA 510(k) Submission Details - K151909

510(k) Number K151909 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 2015
Decision Date April 08, 2016
Days to Decision 270 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
142d slower than avg
Panel avg: 128d · This submission: 270d
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 1375
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K151909.
maxFit II Dental Implant System
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KLOCKNER VEGA DENTAL IMPLANT SYSTEM
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OneQ-SL s-Clean Implant System
K153639 · Dentis Co., Ltd. · Apr 2016
Straumann Bone Level Tapered Implants
K153758 · Institut Straumann AG · Mar 2016