Cleared Traditional

K153099 - INCLUSIVE TAPERED IMPLANT SYSTEM

K153099 is an FDA 510(k) clearance for INCLUSIVE TAPERED IMPLANT SYSTEM, manufactured by Prismatik Dentalcraft, Inc.. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 210-day FDA review.

K153099 · Prismatik Dentalcraft, Inc. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
May 2016
Decision
210d
Days
Class 2
Risk

K153099 is an FDA 510(k) clearance for the INCLUSIVE TAPERED IMPLANT SYSTEM. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Prismatik Dentalcraft, Inc. (Irvine, US). The FDA issued a Cleared decision on May 23, 2016 after a review of 210 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.

FDA 510(k) Submission Details - K153099

510(k) Number K153099 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 26, 2015
Decision Date May 23, 2016
Days to Decision 210 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
82d slower than avg
Panel avg: 128d · This submission: 210d
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 1521
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K153099.
A Plus Internal Fixture System
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Anker II Dental Implant System
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Microdent Ektos Implant System
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IBS Implant System
K153350 · Innobiosurg Co., Ltd. · May 2016
TOUAREG CloseFit™ UNP 2.75mmD
K153111 · Adin Dental Implants Systems , Ltd. · May 2016
K153099 · INCLUSIVE TAPERED IMPLANT SYSTEM
Download PDF FDA Summary Prismatik Dentalcraft…