Cleared Traditional

K945401 - WHITE STAR

K945401 is an FDA 510(k) clearance for WHITE STAR, manufactured by Jeneric/Pentron, Inc.. The device is a Class 2 Dental device with product code EJT cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K945401 · Jeneric/Pentron, Inc. · Dental device
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Dec 1994
Decision
56d
Days
Class 2
Risk

K945401 is an FDA 510(k) clearance for the WHITE STAR. Classified as Alloy, Gold-based Noble Metal (product code EJT), Class II - Special Controls.

Submitted by Jeneric/Pentron, Inc. (Wallingford, US). The FDA issued a Cleared decision on December 29, 1994 after a review of 56 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3060 - 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 Jeneric/Pentron, Inc. devices

FDA 510(k) Submission Details - K945401

510(k) Number K945401 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 03, 1994
Decision Date December 29, 1994
Days to Decision 56 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
71d faster than avg
Panel avg: 127d · This submission: 56d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJT Device Classification - Class 2, Special Controls

Product Code EJT Alloy, Gold-based Noble Metal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3060
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 - EJT Alloy, Gold-based Noble Metal

All 489
Devices cleared under the same product code (EJT) and FDA review panel - the closest regulatory comparables to K945401.
AUROLITE 55
K950858 · Argen Precious Metals, Inc. · Mar 1995
ARGELITE 61 (PALLADIUM - SILVER DENTAL CASTING ALLOY FOR PORCELAIN APPLICATIONS)
K950772 · Argen Precious Metals, Inc. · Mar 1995
ENDURE
K950310 · Aalba Dent, Inc. · Feb 1995
OPULENT 76 AND 83
K945723 · Aalba Dent, Inc. · Dec 1994
QUEST 2 AND 20
K945910 · Aalba Dent, Inc. · Dec 1994
ALLROUND 4
K944889 · J.F. Jelenko & Co., Inc. · Nov 1994