Cleared Traditional

K882126 - JEL-5 GOLD BASED ALLOYS & PRECIOUS METAL ALLOYS

K882126 is an FDA 510(k) clearance for JEL-5 GOLD BASED ALLOYS & PRECIOUS META..., manufactured by J.F. Jelenko & Co., Inc.. The device is a Class 2 Dental device with product code EJT cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K882126 · J.F. Jelenko & Co., Inc. · Dental device
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Jun 1988
Decision
24d
Days
Class 2
Risk

K882126 is an FDA 510(k) clearance for the JEL-5 GOLD BASED ALLOYS & PRECIOUS METAL ALLOYS. Classified as Alloy, Gold-based Noble Metal (product code EJT), Class II - Special Controls.

Submitted by J.F. Jelenko & Co., Inc. (Armonk, US). The FDA issued a Cleared decision on June 13, 1988 after a review of 24 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 J.F. Jelenko & Co., Inc. devices

FDA 510(k) Submission Details - K882126

510(k) Number K882126 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 20, 1988
Decision Date June 13, 1988
Days to Decision 24 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
103d faster than avg
Panel avg: 127d · This submission: 24d
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 551
Devices cleared under the same product code (EJT) and FDA review panel - the closest regulatory comparables to K882126.
ALBABOND 60
K883758 · Degussa Dental, Inc. · Oct 1988
HERA H
K883508 · Degussa Dental, Inc. · Sep 1988
PALLIAG NF III
K883036 · Degussa Dental, Inc. · Aug 1988
OLYMPIA II
K881860 · J.F. Jelenko & Co., Inc. · Jun 1988
PTM-45
K881861 · J.F. Jelenko & Co., Inc. · Jun 1988
PALLADIUM-BASED DENTAL ALLOYS FOR PORCELAIN APPLI.
K880348 · J.F. Jelenko & Co., Inc. · May 1988