Cleared Traditional

K123761 - VITA ENAMIC STAINS

K123761 is an FDA 510(k) clearance for VITA ENAMIC STAINS, manufactured by Innovation Meditech GmbH. The device is a Class 2 Dental device with product code EBD cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K123761 · Innovation Meditech GmbH · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2013
Decision
84d
Days
Class 2
Risk

K123761 is an FDA 510(k) clearance for the VITA ENAMIC STAINS. Classified as Coating, Filling Material, Resin (product code EBD), Class II - Special Controls.

Submitted by Innovation Meditech GmbH (Brea, US). The FDA issued a Cleared decision on March 1, 2013 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3310 - 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 Innovation Meditech GmbH devices

FDA 510(k) Submission Details - K123761

510(k) Number K123761 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 07, 2012
Decision Date March 01, 2013
Days to Decision 84 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
43d faster than avg
Panel avg: 127d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBD Device Classification - Class 2, Special Controls

Product Code EBD Coating, Filling Material, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3310
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 - EBD Coating, Filling Material, Resin

All 42
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