Cleared Traditional

K900209 - WILLI GELLER CERAMIC CREATION & SURPRISE

K900209 is an FDA 510(k) clearance for WILLI GELLER CERAMIC CREATION & SURPRISE, manufactured by Creation North America, Inc.. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 82-day FDA review.

K900209 · Creation North America, Inc. · Dental device
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Apr 1990
Decision
82d
Days
Class 2
Risk

K900209 is an FDA 510(k) clearance for the WILLI GELLER CERAMIC CREATION & SURPRISE. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Creation North America, Inc. (Milwaukee, US). The FDA issued a Cleared decision on April 9, 1990 after a review of 82 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6660 - 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 Creation North America, Inc. devices

FDA 510(k) Submission Details - K900209

510(k) Number K900209 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 17, 1990
Decision Date April 09, 1990
Days to Decision 82 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
45d faster than avg
Panel avg: 127d · This submission: 82d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EIH Device Classification - Class 2, Special Controls

Product Code EIH Powder, Porcelain
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.6660
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 - EIH Powder, Porcelain

All 454
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K900209.
PV-CERAMIC, CERAMINIQUE
K901261 · Ivoclar North America, Inc. · Jun 1990
OPAQUE PORCELAIN
K900393 · Dentsply Intl. · Apr 1990
SILHOUETTE PORCELAIN
K895888 · Leach and Dillon Co., Inc. · Apr 1990
SHAKE N' SPRAY (W/SILHOUETTE PORCELAIN)
K895889 · Leach and Dillon Co., Inc. · Apr 1990
DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES
K853707 · Dentsply Intl. · Nov 1985
SCOTCHPRIME CERAMIC PRIMER
K853698 · 3M Company · Nov 1985