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.

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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: EFD FDA class 1

Amalgamator, Dental, Ac-Powered

Dental

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The AC-Powered Dental Amalgamator is a dental device that uses electrical power to mix amalgam alloy powder and mercury in a capsule through high-speed vibration, producing a homogeneous amalgam for use as a tooth filling material. It is classified as FDA Class 1, the lowest risk category, subject only to general controls and no premarket submission is required. The product code is EFD and the applicable regulation is 21 CFR 872.3100, under the Dental medical specialty.

510(k) Clearances

15 matches
K Number
Device Name
PENTAMIX 2
SILIMAT PLUS
IPT CAPSULE MIXER
AUTOMIX DENTAL AMALGAMATOR
DUOMAT 3 AMALGAMATOR
MIXOMAT AMALGAMATOR
DENTOMAT 3 AMALGAMATORS
ACCU-MIX AMALGAMATOR
SILAMAT (AMALGAMATOR)
DRILLING MACHINE W/HANDPIECES & INTERNAL IRRIGA.
ESPE CAPMIX
AMALGAMATOR
AMALGAMATOR MODEL SDC--
DENTAL AMALGAMATOR
CAPMIX

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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