Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: EJJ FDA class 2

Alloy, Amalgam

Dental

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Amalgam Alloy is a dental restorative material consisting of a silver-based alloy powder, historically combined with mercury to form a plastic amalgam mass that hardens into a durable restorative for posterior teeth. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket clearance and compliance with special controls given material biocompatibility considerations. The product code is EJJ, regulated under 21 CFR 872.3070 in the Dental (DE) specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
SILVERFIL
SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70
BESTALOY
BENCO ADMIX
BENCO SPHERICAL
HIGH SILVER CONVENTIONAL
FUTURA TOPCAP NON GAMMA-2
ANA 3000 SM NON GAMMA 2 MODIFIED SPHERICAL DENTAL ALLOY
ANA 70 NON GAMMA 2 DISPERSED PHASE DENTAL ALLOY
ANA 2000 NON GAMMA 2 EXTRA HIGH COPPER DENTAL ALLOY
PARAGON
SECURALLOY
VIVACAP HR
AMALCAP PLUS
VIVALLOY HR
CENTURY ALLOY
PLA-96P
PLS-96P
ARDENT NON GAMMA-2 70
ARDENT FUTURA NON GAMMA-2
GALLOY
CUPRALLOY
TYTIN R
ULTRA SPHERICAL AMALGAM ALLOY
TYTIN ADMIX
AGALLOY, DISALLOY, EPSILON AND LAMBDA
SYBRALOY
TYTIN
INDIPERSE
PRINCE
DISPOSABLE TURP FLUID CONTAINMENT DRAPE - STERILE
GK DENTAL AMALGAM ALLOY
ANA 70 DISPERSED PHASE DENTAL ALLOY -- MODIFIED
AMALGAPHASE
KERALLOY-D CAPS
MIRACLE MIX CAPS GLASS IONOMER CEMENT INCAPSULES
KERALLOY NON-GAMMA 2 AMALGAM
DW 236
DW 235
LUXALLOY 50 (POWDER, TABLETS, PREDOSED CAPSULES)
LUXALLOY CAPS (PREDOSED CAPSULES)
ARTALLOY (POWDER)
VIVAALLOY HR (AMALGAM)
AMALCAP PLUS
PENT CAPS
OROSPHERE PLUS
OROSPHERE HCDP
GK ALLOY
OLYMPIA ALLOY
HERAEUS' HERAGAM 48, NON GAMMA 2 DEN. AMAL. ALLOY

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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