Cleared Traditional

K982665 - JUMBO SILVER-REINFORCED GLASS IONOMER

K982665 is the FDA 510(k) clearance for JUMBO SILVER-REINFORCED GLASS IONOMER by Centrix, Inc.. It is a Class 2 Dental device (product code EMA) cleared through the Traditional 510(k) pathway after a 46-day FDA review.

K982665 · Centrix, Inc. · Dental device
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Sep 1998
Decision
46d
Days
Class 2
Risk

K982665 is an FDA 510(k) clearance for the JUMBO SILVER-REINFORCED GLASS IONOMER. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Centrix, Inc. (Shelton, US). The FDA issued a Cleared decision on September 8, 1998 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 Centrix, Inc. devices

Submission Details

510(k) Number K982665 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 24, 1998
Decision Date September 08, 1998
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.

Device Classification

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 286
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K982665.
ZINFOS ZINC PHOSPHATE CEMENT
K982913 · Scientific Pharmaceuticals, Inc. · Oct 1998
TEMPBOND CLEAR-2
K982590 · Sybron Dental Specialties, Inc. · Oct 1998
STERI-OSS' IMPROV TEMPORARY DENTAL CEMENT
K982400 · Steri-Oss, Inc. · Sep 1998
GLASIONOMER CEMENT CX PLUS
K982461 · Shofu Dental Corp. · Aug 1998
LIQUID A
K981618 · Harry J. Bosworth Co. · Jul 1998
FLOWABLE COMPOSITE
K981965 · Dentsply Intl. · Jul 1998