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: DYN FDA class 1

Mouthpiece, Saliva Ejector

Dental

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The Saliva Ejector Mouthpiece is a dental device attached to a suction system and placed in the patient's mouth to continuously remove saliva, blood, and water during dental procedures, keeping the oral field clear. 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 DYN and the applicable regulation is 21 CFR 872.6640, under the Dental medical specialty.

510(k) Clearances

18 matches
K Number
Device Name
DENTFLEX DISPLOSABLE DENTAL SALIVA EJECTOR
SALIVA EJECTOR DISPOSABLE
HYGOFLEX SALIVA-EJECTOR
EJECTOR
HIGH VAC
MINIDAM
SALIVA ABSORBER - DENTAL
ORAL ASPIRATOR
TIP, DENTAL SUCTION APPARATUS
SILIVA EJECTOR/ORAL CAVITY EVACUATOR
SALIVA EJECTORS
ULS 8-86
SALIVA EJECTOR
SILENTSLEEP
TONGUE HOLDER/SALIVA EJECTOR
SURGICAL ASPIRATOR TIPS
OPTIONS FOR STAR DENTAL OPUS I
SALIVA EJECTOR

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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