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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

Free to try · every answer cites its records

Product Code: EJH FDA class 2

Alloy, Metal, Base

Dental

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The Base Metal Alloy is a dental casting material composed primarily of non-precious metals such as nickel, chromium, cobalt, or beryllium alloys, used in the fabrication of metal copings, crowns, bridges, and removable partial denture frameworks. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket clearance. The product code is EJH, regulated under 21 CFR 872.3710 in the Dental (DE) specialty.

510(k) Clearances

50+ matches
K Number
Device Name
BEGOPAL+
CONTINUM V
CONTINUM
VERASOFT ES
DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECAST
WIROBOND C
NANO-TICROWN
PD CASTA-H
CERACAST-V
SUPERBOND
KAVO EVEREST TITANBLANK
GOLD CORE PLUS
JEWEL CAST PLUS
BIOLOY
CERALOY
CHROLOY
CHROLOY SOLDER
CERALOY SOLDER
4 ALL (DW286A)
D.SIGN 15 (DW286 B)
PISCES PLUS (DW286 C)
XERAFIT
FLEXICAST PRIME
SUPREMCAST
D.SIGN 30
DURABOND NON-PRECIOUS CERAMIC ALLOY
AUROFILM NP
FLEXICAST
JEWEL CAST III
GOLD CORE II
SUPER 6
SUPER 14
SUPER 12
SUPER 3
SUPER 1
DC TITAN
SUPREMCAST V
DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC
CERAMIX EZ CAST, CERAMIX EZ CAST SOLDER, CERAMIX EZ CAST FLUX
CERADIUM V NON-PRECIOUS CERAMIC ALLOY
HI BOND NON-PRECIOUS CERAMIC ALLOY
P10 SPECIAL
CERADIUM NON-PRECIOUS CERAMIC ALLOY
D-SIGN V (R&D PROJECT DW267#17)
D-SIGN VI (R&D PROJECT DW266#9)
JELBOND NP
VERABOND 2
NPG + 2
SOWELL NICKEL-CHROME-MOLYBDENUM ALLOY
SOWELL NICKEL-CHROME NON-PRECIOUS METAL 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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