Cleared Traditional

K942665 - ORTHOCENT: LIQUID AND POWDER

K942665 is an FDA 510(k) clearance for ORTHOCENT: LIQUID AND POWDER, manufactured by Dentauraum, Inc.. The device is a Class 2 Dental device with product code EMA cleared through the Traditional 510(k) pathway after a 46-day FDA review.

K942665 · Dentauraum, Inc. · Dental device
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Jul 1994
Decision
46d
Days
Class 2
Risk

K942665 is an FDA 510(k) clearance for the ORTHOCENT: LIQUID AND POWDER. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Dentauraum, Inc. (Newtown, US). The FDA issued a Cleared decision on July 22, 1994 after a review of 46 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 Dentauraum, Inc. devices

FDA 510(k) Submission Details - K942665

510(k) Number K942665 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 06, 1994
Decision Date July 22, 1994
Days to Decision 46 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
81d faster than avg
Panel avg: 127d · This submission: 46d
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 309
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K942665.
PULP CANAL SEALER EWT
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K935436 · Wallace A. Erickson & Co. · Jun 1994