Cleared Traditional

K151723 - Rainbow Trans

K151723 is an FDA 510(k) clearance for Rainbow Trans, manufactured by Genoss. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 124-day FDA review.

K151723 · Genoss · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2015
Decision
124d
Days
Class 2
Risk

K151723 is an FDA 510(k) clearance for the Rainbow Trans. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Genoss (Suwon-Si, KR). The FDA issued a Cleared decision on October 28, 2015 after a review of 124 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6660 - 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.

View all Genoss devices

FDA 510(k) Submission Details - K151723

510(k) Number K151723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 26, 2015
Decision Date October 28, 2015
Days to Decision 124 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
3d faster than avg
Panel avg: 127d · This submission: 124d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EIH Device Classification - Class 2, Special Controls

Product Code EIH Powder, Porcelain
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.6660
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 - EIH Powder, Porcelain

All 291
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K151723.
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