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: EGG FDA class 1

Attachment, Precision, All

Dental

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The Precision Attachment is a dental prosthetic device consisting of interlocking male and female components used to connect removable partial dentures or overdentures to abutment teeth or implants with a precise, retentive fit, providing improved stability compared to conventional clasps. 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 EGG and the applicable regulation is 21 CFR 872.3165, under the Dental medical specialty.

510(k) Clearances

24 matches
K Number
Device Name
STECO-TITANMAGNETICS
COUPLING DEVICE FOR DENTAL PROSTHESIS
ZEST ANCHOR ADVANCED GENERATION
COGAN CORP KITS OF DENTAL HAND INSTRUMENTS
DENTAL CONNECTOR PRECISION ATTACHMENT
CONICAST, INTRACAST, OMECAST
INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH
MICRO 2 SYSTEM
DENTAL BRIDGE ANCHORING PINS
PRECISION DENTAL ATTACHMENTS
T.R.S.: TOOTH REPLACEMENT SYSTEM
MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER
COSMETIC SINGLE SPAN BRIDGE
IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS
SHINER STRESS DIRECTING ATTACHMENT
ZEST MARK II (STANDARD & MINI)
DYNA SYSTEM
JACKSON RARE EARTH MAGNETIC ATTACHMENT
MAGNE-DENT
DENTA A-33
DISTAFLEX
PRECIOUS-METAL/PLASTIC ATTACH., AUXILL
MICRO-RING SYSTEM PRECISION ATTACH.
MICRO-RING

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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