Cleared Special

White Endoseal MTA (K212229) - FDA 510(k) Clearance

Class II Dental device cleared through the Special 510(k) pathway - typically does not require clinical trials.

K212229 · Maruchi · Dental device
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Optimized for regulatory review, auditing and printing
Aug 2021
Decision
28d
Days
Class 2
Risk

K212229 is an FDA 510(k) clearance for the White Endoseal MTA. Classified as Resin, Root Canal Filling (product code KIF), Class II - Special Controls.

Submitted by Maruchi (Wonju-Si, KR). The FDA issued a Cleared decision on August 13, 2021 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3820 - the FDA dental device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Maruchi devices

Submission Details

510(k) Number K212229 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 16, 2021
Decision Date August 13, 2021
Days to Decision 28 days
Submission Type Special
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
99d faster than avg
Panel avg: 127d · This submission: 28d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code KIF Resin, Root Canal Filling
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3820
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 - KIF Resin, Root Canal Filling

All 58
Devices cleared under the same product code (KIF) and FDA review panel - the closest regulatory comparables to K212229.
UltraCal XS
K211905 · Ultradent Products, Inc. · Oct 2021
BioRoot Flow 0.5g, BioRoot Flow 2g
K212283 · Septodont · Sep 2021
Sonendo Filling Material 5C
K211995 · Sonendo, Inc. · Aug 2021
Biodentine XP 500, Biodentine XP 200
K211799 · Septodont · Aug 2021
Metapaste Plus
K210904 · Meta Biomed Co., Ltd. · Jun 2021
Metapex Plus
K202617 · Meta Biomed Co., Ltd. · Apr 2021