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: EJT FDA class 2

Alloy, Gold-Based Noble Metal

Dental

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Gold-Based Noble Metal Alloy is a high-gold-content dental casting material used to fabricate inlays, onlays, crowns, and bridges valued for their excellent biocompatibility, corrosion resistance, ease of casting, and long-term clinical performance. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket clearance. The product code is EJT, regulated under 21 CFR 872.3060 in the Dental (DE) specialty.

510(k) Clearances

50+ matches
K Number
Device Name
PROMETAL HN86
BIO 60
PORTA REFLEX
PORTA SOLDER 1090 W
NDX-40 ALLOY
HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORM
GOLD DENTAL CASTING ALLOYS
APEX93, APEX87, APEX84, APEX85, APEX77, E-SARANG 88 AND E-SARANG 82
E-SARANG 86, DM78, DM55
APPOLLO 3 ALLOY
ORION E ALLOY
CERA R PLUS ALLOY
MINERVA 58 ALLOY
ORION GX ALLOY
CERA F ALLOY
ULTRACROWN 75 ALLOY
DW 296 #15 SOLDER
R&D DESIGNATION AP-052-5
ALEXANDER
STARBOND DENTAL BONDING ALLOYS
MIRACLE 98
PORTA PRESSOVER
STARCAST DENTAL ALLOYS
BIO UNIVERSAL
BIOUNIVERSAL PKF
PORTA IMPLANT
AIGIS-FINE
AIGIS-SUPER
AIGIS-SOFT
AIGIS-PLUS
AIGIS-XO
AIGIS-INLAY
AIGIS-PT
NEO 76
AIGIS-A
APEX 90
UCP DENTAL MATERIAL
UCC DENTAL MATERIAL
GOLD CORE 35
PORTADUR P2
BIOPORTA G
PORTA GEO TI
AGC SPECIAL ALLOY
CERANUM 82
CERANUM 50
CERANUM 76
CERANUM 90
LUCIUS 76
KERADEC
UNIVERSAL CERAMIC SOLDER

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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