Cleared Traditional

K932893 - VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY

K932893 is an FDA 510(k) clearance for VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY, manufactured by Vident. The device is a Class 2 Dental device with product code EJH cleared through the Traditional 510(k) pathway after a 291-day FDA review.

K932893 · Vident · Dental device
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Mar 1994
Decision
291d
Days
Class 2
Risk

K932893 is an FDA 510(k) clearance for the VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY. Classified as Alloy, Metal, Base (product code EJH), Class II - Special Controls.

Submitted by Vident (Baldwin Park, US). The FDA issued a Cleared decision on March 28, 1994 after a review of 291 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3710 - 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.

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FDA 510(k) Submission Details - K932893

510(k) Number K932893 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 10, 1993
Decision Date March 28, 1994
Days to Decision 291 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
164d slower than avg
Panel avg: 127d · This submission: 291d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJH Device Classification - Class 2, Special Controls

Product Code EJH Alloy, Metal, Base
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3710
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 - EJH Alloy, Metal, Base

All 99
Devices cleared under the same product code (EJH) and FDA review panel - the closest regulatory comparables to K932893.
VERABOND V
K945712 · Aalba Dent, Inc. · Dec 1994
VERABOND II
K945713 · Aalba Dent, Inc. · Dec 1994
VERABOND III
K945714 · Aalba Dent, Inc. · Dec 1994
LPG 5/10, LPG 10/5, LPG 10/15 AND LPG 15/10
K940749 · Aalba Dent, Inc. · Mar 1994
R2+
K934758 · Jeneric/Pentron, Inc. · Feb 1994
ARGELOY PARTIAL (NON-PRECIOUS)
K935829 · Argen Precious Metals, Inc. · Jan 1994