Cleared Traditional

K930868 - DYNA IMPLANT DESIGN

K930868 is an FDA 510(k) clearance for DYNA IMPLANT DESIGN, manufactured by Dyna Dental Engineering BV. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 798-day FDA review.

K930868 · Dyna Dental Engineering BV · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1995
Decision
798d
Days
Class 2
Risk

K930868 is an FDA 510(k) clearance for the DYNA IMPLANT DESIGN. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Dyna Dental Engineering BV (2594 Ac Den Haag-Holland, NU). The FDA issued a Cleared decision on April 28, 1995 after a review of 798 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 Dyna Dental Engineering BV devices

FDA 510(k) Submission Details - K930868

510(k) Number K930868 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 19, 1993
Decision Date April 28, 1995
Days to Decision 798 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
671d slower than avg
Panel avg: 127d · This submission: 798d
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 1319
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K930868.
INTEGRAL VI BIOINTEGRATED DENTAL IMPLANT SYSTEM
K944327 · Calcitek, Inc. · May 1995
INTEGRAL OMNILOC DENTAL IMPLANT WITH INTERFACE RING
K941608 · Calcitek, Inc. · May 1995
BONE CUTTING INSTRUMENT AND ACCESSORIES
K950446 · Steri-Oss, Inc. · May 1995
KIS-II STR FIXTURES
K944725 · Implant Center of the Palm Beaches · Apr 1995
BONE CUTTING INSTRUMENT AND ACCESSORIES
K950936 · Steri-Oss, Inc. · Apr 1995
STERI-OSS SCALER FOR DENTAL IMPLANTS
K943681 · Steri-Oss, Inc. · Apr 1995