Cleared Traditional

K172701 - BIO-C SEALER

K172701 is an FDA 510(k) clearance for BIO-C SEALER, manufactured by Angelus Industria DE Produtos Odontologicos S/A. The device is a Class 2 Dental device with product code KIF cleared through the Traditional 510(k) pathway after a 119-day FDA review.

K172701 · Angelus Industria DE Produtos Odontologicos S/A · Dental device
Download Printable Device Report (PDF)
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Jan 2018
Decision
119d
Days
Class 2
Risk

K172701 is an FDA 510(k) clearance for the BIO-C SEALER. Classified as Resin, Root Canal Filling (product code KIF), Class II - Special Controls.

Submitted by Angelus Industria DE Produtos Odontologicos S/A (Londrina, BR). The FDA issued a Cleared decision on January 4, 2018 after a review of 119 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3820 - 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 Angelus Industria DE Produtos Odontologicos S/A devices

FDA 510(k) Submission Details - K172701

510(k) Number K172701 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 07, 2017
Decision Date January 04, 2018
Days to Decision 119 days
Submission Type Traditional
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
8d faster than avg
Panel avg: 127d · This submission: 119d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KIF Device Classification - Class 2, Special Controls

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 83
Devices cleared under the same product code (KIF) and FDA review panel - the closest regulatory comparables to K172701.
BIO-C REPAIR
K180185 · Angelus Industria DE Produtos Odontologicos S/A · Aug 2018
ENDOSEAL MTA
K170175 · Maruchi · Feb 2018
ENDOSOLV
K172839 · Septodont · Feb 2018
PROROOT MTA WHITE, PROROOT MTA GRAY
K142178 · Dentsply International, Inc. · Feb 2015
REALSEAL XT SEALER
K102163 · Kerr Corporation · Oct 2010
ENDOREZ OBTURATION KIT (WITH ACCELERATOR), MODEL 403, ENDOREZ ACCELERATOR (REFILL), MODEL 399
K071106 · Ultradent Products, Inc. · May 2007