Cleared Traditional

K040807 - MIS DENTAL IMPLANT SYSTEM

K040807 is an FDA 510(k) clearance for MIS DENTAL IMPLANT SYSTEM, manufactured by Mis - Implant Technologies , Ltd.. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 72-day FDA review.

K040807 · Mis - Implant Technologies , Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2004
Decision
72d
Days
Class 2
Risk

K040807 is an FDA 510(k) clearance for the MIS DENTAL IMPLANT SYSTEM. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Mis - Implant Technologies , Ltd. (Elmwood Park, US). The FDA issued a Cleared decision on June 9, 2004 after a review of 72 days - a notably fast clearance 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Mis - Implant Technologies , Ltd. devices

FDA 510(k) Submission Details - K040807

510(k) Number K040807 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 29, 2004
Decision Date June 09, 2004
Days to Decision 72 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
55d faster than avg
Panel avg: 127d · This submission: 72d
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 895
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K040807.
ANKYLOS DENTAL IMPLANT SYSTEM
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STRAUMANN DENTAL IMPLANT SYSTEM
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LORENZ SELF-DRILLING IMF SCREW
K040983 · Walter Lorenz Surgical, Inc. · May 2004
SPI CONTACT DENTAL IMPLANT
K034014 · Thommen Medical AG · Mar 2004