Cleared Traditional

K870148 - DURA ORTHO ACRYLIC

K870148 is an FDA 510(k) clearance for DURA ORTHO ACRYLIC, manufactured by Reliance Dental Mfg. Co.. The device is a Class 2 Dental device with product code EBI cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K870148 · Reliance Dental Mfg. Co. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1987
Decision
37d
Days
Class 2
Risk

K870148 is an FDA 510(k) clearance for the DURA ORTHO ACRYLIC. Classified as Resin, Denture, Relining, Repairing, Rebasing (product code EBI), Class II - Special Controls.

Submitted by Reliance Dental Mfg. Co. (Worth, US). The FDA issued a Cleared decision on February 19, 1987 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3760 - 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 Reliance Dental Mfg. Co. devices

FDA 510(k) Submission Details - K870148

510(k) Number K870148 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 13, 1987
Decision Date February 19, 1987
Days to Decision 37 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
91d faster than avg
Panel avg: 128d · This submission: 37d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBI Device Classification - Class 2, Special Controls

Product Code EBI Resin, Denture, Relining, Repairing, Rebasing
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3760
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 - EBI Resin, Denture, Relining, Repairing, Rebasing

All 265
Devices cleared under the same product code (EBI) and FDA review panel - the closest regulatory comparables to K870148.
LIGHT CURE DENTURE GLAZE
K871849 · Austenal Dental, Inc. · Aug 1987
AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL
K863630 · Austenal Dental, Inc. · Mar 1987
AUSTENAL ACUSOFT SOFT LINER
K862557 · Austenal Dental, Inc. · Feb 1987
TRIAD IMPACT
K863324 · Dentsply Intl. · Sep 1986
AUSTENAL ACUPAC HI DENTURE BASE MATERIAL
K862558 · Austenal Dental, Inc. · Jul 1986
ACRYLIC SOLDER
K861239 · Parker Laboratories, Inc. · Apr 1986