Cleared Traditional

K122807 - DENTAL IMPLANT SYSTEM

K122807 is an FDA 510(k) clearance for DENTAL IMPLANT SYSTEM, manufactured by Hager& Meisinger GmbH. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 652-day FDA review.

K122807 · Hager& Meisinger GmbH · Dental device
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Jun 2014
Decision
652d
Days
Class 2
Risk

K122807 is an FDA 510(k) clearance for the DENTAL IMPLANT SYSTEM. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Hager& Meisinger GmbH (Centennial, US). The FDA issued a Cleared decision on June 13, 2014 after a review of 652 days - an unusually long review period, suggesting complex equivalence evaluation.

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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Dental submissions.

View all Hager& Meisinger GmbH devices

FDA 510(k) Submission Details - K122807

510(k) Number K122807 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 2012
Decision Date June 13, 2014
Days to Decision 652 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
525d slower than avg
Panel avg: 127d · This submission: 652d
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 759
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K122807.
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K133339 · Zimmer Dental, Inc. · Mar 2014
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K132258 · Zimmer Dental, Inc. · Nov 2013