Cleared Traditional

K854702 - PLASTIC MOUNTING RINGS

K854702 is an FDA 510(k) clearance for PLASTIC MOUNTING RINGS, manufactured by Almore Intl., Inc.. The device is a Class 1 Dental device with product code EJP cleared through the Traditional 510(k) pathway after a 105-day FDA review.

K854702 · Almore Intl., Inc. · Dental device
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Mar 1986
Decision
105d
Days
Class 1
Risk

K854702 is an FDA 510(k) clearance for the PLASTIC MOUNTING RINGS. Classified as Articulators (product code EJP), Class I - General Controls.

Submitted by Almore Intl., Inc. (Portland, US). The FDA issued a Cleared decision on March 6, 1986 after a review of 105 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3150 - 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 Almore Intl., Inc. devices

FDA 510(k) Submission Details - K854702

510(k) Number K854702 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 21, 1985
Decision Date March 06, 1986
Days to Decision 105 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
22d faster than avg
Panel avg: 127d · This submission: 105d
Pathway characteristics
Predicate-based equivalence.

EJP Device Classification - Class 1, General Controls

Product Code EJP Articulators
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.3150
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - EJP Articulators

Devices cleared under the same product code (EJP) and FDA review panel - the closest regulatory comparables to K854702.
GNATHOMAT ARTICULATOR
K896131 · Ivoclar North America, Inc. · Dec 1989
DISPOSABLE ARTICULATOR
K872943 · Dentsply Intl. · Aug 1987
GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX
K863009 · Sds Dental, Inc. · Sep 1986
HANDY IIM
K833039 · Shofu Dental Corp. · Oct 1983
BALANCE ARTICULATOR
K811075 · Almore Intl., Inc. · May 1981
DISPOSABLE ARTICULATOR
K801342 · Williams Gold Refining Co., Inc. · Jul 1980