Cleared Traditional

K964808 - SPETEMP

K964808 is an FDA 510(k) clearance for SPETEMP, manufactured by Ultradent Products, Inc.. The device is a Class 2 Dental device with product code EMA cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K964808 · Ultradent Products, Inc. · Dental device
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Feb 1997
Decision
89d
Days
Class 2
Risk

K964808 is an FDA 510(k) clearance for the SPETEMP. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Ultradent Products, Inc. (South Jordan, US). The FDA issued a Cleared decision on February 26, 1997 after a review of 89 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3275 - 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 Ultradent Products, Inc. devices

FDA 510(k) Submission Details - K964808

510(k) Number K964808 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 29, 1996
Decision Date February 26, 1997
Days to Decision 89 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
38d faster than avg
Panel avg: 127d · This submission: 89d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EMA Device Classification - Class 2, Special Controls

Product Code EMA Cement, Dental
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3275
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 - EMA Cement, Dental

All 421
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K964808.
HI DENSE TC
K971927 · Shofu Dental Corp. · Jun 1997
TEMPOCEM NE (MULTIPLE)
K970774 · Foremost Dental Mfg., Inc. · Jun 1997
TEMPO CEM (MULTIPLE)
K970775 · Foremost Dental Mfg., Inc. · Jun 1997
DENTEMP ONE STEP
K964773 · Majestic Drug Co., Inc. · Feb 1997
SPETEMP EF
K964809 · Ultradent Products, Inc. · Jan 1997
HYCEM APLICAP
K963737 · Espe GmbH & Co. Kg. · Nov 1996