Cleared Traditional

K864707 - SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH

K864707 is an FDA 510(k) clearance for SR-VIVODENT ANTERIOR & SR-ORTHOTYP POST..., manufactured by Ivoclar USA, Inc.. The device is a Class 2 Dental device with product code ELM cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K864707 · Ivoclar USA, Inc. · Dental device
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Feb 1987
Decision
70d
Days
Class 2
Risk

K864707 is an FDA 510(k) clearance for the SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH. Classified as Denture, Plastic, Teeth (product code ELM), Class II - Special Controls.

Submitted by Ivoclar USA, Inc. (Chicago, US). The FDA issued a Cleared decision on February 10, 1987 after a review of 70 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3590 - 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 Ivoclar USA, Inc. devices

FDA 510(k) Submission Details - K864707

510(k) Number K864707 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 02, 1986
Decision Date February 10, 1987
Days to Decision 70 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
57d faster than avg
Panel avg: 127d · This submission: 70d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ELM Device Classification - Class 2, Special Controls

Product Code ELM Denture, Plastic, Teeth
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3590
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 - ELM Denture, Plastic, Teeth

All 32
Devices cleared under the same product code (ELM) and FDA review panel - the closest regulatory comparables to K864707.
NEW TOOTH MATERIAL
K920684 · Dentsply Intl. · Dec 1992
VITAPAN ACRYLIC DENTURE TEETH
K914476 · Vident · Mar 1992
DENTURE PLASTIC TEETH,76 ELM
K915276 · Nobelpharma USA, Inc. · Feb 1992
AUSTENAL MODIFIED ACRYLIC DENTURE RESIN
K853160 · Austenal Dental, Inc. · Oct 1985
DELTA TEETH
K831214 · Dentsply Intl. · May 1983
TEETH, DENTURE, PLASTIC
K792245 · Dentsply Intl. · Jan 1980