Cleared Traditional

K141503 - DENALI 501CEMENT

K141503 is an FDA 510(k) clearance for DENALI 501CEMENT, manufactured by Denali Corporation. The device is a Class 2 Dental device with product code EMA cleared through the Traditional 510(k) pathway after a 157-day FDA review.

K141503 · Denali Corporation · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 2014
Decision
157d
Days
Class 2
Risk

K141503 is an FDA 510(k) clearance for the DENALI 501CEMENT. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Denali Corporation (Hanover, US). The FDA issued a Cleared decision on November 10, 2014 after a review of 157 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3275 - 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 Denali Corporation devices

FDA 510(k) Submission Details - K141503

510(k) Number K141503 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 06, 2014
Decision Date November 10, 2014
Days to Decision 157 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
30d slower than avg
Panel avg: 127d · This submission: 157d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EMA Device Classification - Class 2, Special Controls

Product Code EMA Cement, Dental
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3275
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 - EMA Cement, Dental

All 353
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K141503.
Bifix Temp
K143212 · Voco GmbH · May 2015
PANAVIA SA Cement Plus Handmix
K142623 · Kuraray Noritake Dental, Inc. · Feb 2015
PANAVIA SA Cement Plus Automix
K142625 · Kuraray Noritake Dental, Inc. · Jan 2015
IONOSTAR MOLAR
K140993 · Voco GmbH · Oct 2014
ESTEMP IMPLANT, ESTEMP CLEAR
K134021 · Spident Co., Ltd. · Jun 2014
MULTILINK HYBRID ABUTMENT CEMENT
K130436 · Ivoclar Vivadent, AG · Aug 2013