Cleared Traditional

K020376 - AHL GENERIC GLASS IONOMER AESTHETIC RES...

K020376 is an FDA 510(k) clearance for AHL GENERIC GLASS IONOMER AESTHETIC RES..., manufactured by Advanced Healthcare , Ltd.. The device is a Class 2 Dental device with product code EMA cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K020376 · Advanced Healthcare , Ltd. · Dental device
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Apr 2002
Decision
64d
Days
Class 2
Risk

K020376 is an FDA 510(k) clearance for the AHL GENERIC GLASS IONOMER AESTHETIC RESTORATIVE. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Advanced Healthcare , Ltd. (Sylmar, US). The FDA issued a Cleared decision on April 9, 2002 after a review of 64 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 Advanced Healthcare , Ltd. devices

FDA 510(k) Submission Details - K020376

510(k) Number K020376 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 04, 2002
Decision Date April 09, 2002
Days to Decision 64 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
63d faster than avg
Panel avg: 127d · This submission: 64d
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 321
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K020376.
RELYX RMGIP
K022476 · 3M Company · Aug 2002
GC ELITE CEMENT 100
K021038 · GC America, Inc. · May 2002
PULPDENT POST CEMENT
K020481 · Pulpdent Corporation · Apr 2002
UNICEM
K020256 · 3M Espe AG Dental Products · Mar 2002
GC FUJI LINING LC PASTE PAK
K020117 · GC America, Inc. · Feb 2002
SCI-PHARM POST SECURE
K013555 · Scientific Pharmaceuticals, Inc. · Jan 2002