Cleared Traditional

K962333 - V.R.S. DENTURE RESIN MATERIAL

K962333 is the FDA 510(k) clearance for V.R.S. DENTURE RESIN MATERIAL by Vident. It is a Class 2 Dental device (product code EBI) cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K962333 · Vident · Dental device
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Aug 1996
Decision
51d
Days
Class 2
Risk

K962333 is an FDA 510(k) clearance for the V.R.S. DENTURE RESIN MATERIAL. Classified as Resin, Denture, Relining, Repairing, Rebasing (product code EBI), Class II - Special Controls.

Submitted by Vident (Brea, US). The FDA issued a Cleared decision on August 7, 1996 after a review of 51 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 Vident devices

Submission Details

510(k) Number K962333 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 17, 1996
Decision Date August 07, 1996
Days to Decision 51 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
76d faster than avg
Panel avg: 127d · This submission: 51d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 140
Devices cleared under the same product code (EBI) and FDA review panel - the closest regulatory comparables to K962333.
TRUBYTE SOFT RELINE SYSTEM
K964040 · Dentsply Intl. · Dec 1996
SOFT DENTURE REBASING RESIN
K963736 · Sybron Dental Specialties, Inc. · Dec 1996
GC BASELINE
K963144 · GC America, Inc. · Oct 1996
QUICKSPLINT
K961995 · Heraeus Kulzer, Inc. · Jun 1996
BOSWORTH LIQUID RESIN II
K961200 · Harry J. Bosworth Co. · May 1996
CONNECT
K954689 · Sybron Dental Specialties, Inc. · Oct 1995