Cleared Traditional

K872510 - DEN-MAT TENURE

K872510 is an FDA 510(k) clearance for DEN-MAT TENURE, manufactured by Den-Mat Corp.. The device is a Class 2 Dental device with product code EBF cleared through the Traditional 510(k) pathway after a 61-day FDA review.

K872510 · Den-Mat Corp. · Dental device
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Aug 1987
Decision
61d
Days
Class 2
Risk

K872510 is an FDA 510(k) clearance for the DEN-MAT TENURE. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Den-Mat Corp. (Santa Maria, US). The FDA issued a Cleared decision on August 24, 1987 after a review of 61 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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 Den-Mat Corp. devices

FDA 510(k) Submission Details - K872510

510(k) Number K872510 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 1987
Decision Date August 24, 1987
Days to Decision 61 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 127d · This submission: 61d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBF Device Classification - Class 2, Special Controls

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
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 - EBF Material, Tooth Shade, Resin

All 798
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K872510.
LEE COMPOSITE INLAY SYSTEM
K873123 · Lee Pharmaceuticals · Jan 1988
CLEARFIL PORCELAIN REPAIR SYSTEM
K873886 · Kuraray Co. · Nov 1987
SILUX PLUS LIGHT CURED RESTORATIVE MATERIAL
K872444 · 3M Company · Sep 1987
CLEARFIL POSTERIOR NEW BOND
K872960 · Kuraray Co. · Aug 1987
SYNERGY
K872890 · Scientific Pharmaceuticals, Inc. · Aug 1987
DENTIN ADHESIVE
K872907 · Dentsply Intl. · Aug 1987