Cleared Traditional

K813418 - INZOMA NP

K813418 is an FDA 510(k) clearance for INZOMA NP, manufactured by J. Aderer, Inc.. The device is a Class 2 Dental device with product code EJS cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K813418 · J. Aderer, Inc. · Dental device
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Jan 1982
Decision
31d
Days
Class 2
Risk

K813418 is an FDA 510(k) clearance for the INZOMA NP. Classified as Alloy, Other Noble Metal (product code EJS), Class II - Special Controls.

Submitted by J. Aderer, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 7, 1982 after a review of 31 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. Aderer, Inc. devices

FDA 510(k) Submission Details - K813418

510(k) Number K813418 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 07, 1981
Decision Date January 07, 1982
Days to Decision 31 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
96d faster than avg
Panel avg: 127d · This submission: 31d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJS Device Classification - Class 2, Special Controls

Product Code EJS Alloy, Other 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 - EJS Alloy, Other Noble Metal

All 156
Devices cleared under the same product code (EJS) and FDA review panel - the closest regulatory comparables to K813418.
CLASS OF CASTING ALLOYS TYPE III OR ALT
K820434 · Howmedica Corp. · Mar 1982
CLASS OF PRECIOUS METAL CASTING ALLOYS
K820407 · Howmedica Corp. · Mar 1982
CLASS OF CASTING ALLOYS TYPE IV OR ALT
K820408 · Howmedica Corp. · Mar 1982
BAK-ON SP PORCELAIN ALLOY
K812101 · Johnson & Johnson Professionals, Inc. · Aug 1981
PRESOLDER FOR NON-PRECIOUS DENTAL ALLOYS
K811563 · Williams Gold Refining Co., Inc. · Jul 1981
HOWMEDICA T-III G ALLOY
K810380 · Howmedica Corp. · Mar 1981