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: EHZ FDA class 1

Evacuator, Oral Cavity

Dental

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The Oral Cavity Evacuator is a dental device, such as a suction tip or saliva ejector, connected to a vacuum system to remove fluids, blood, saliva, and debris from the oral cavity during dental procedures, maintaining a clear working field. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is EHZ, regulated under 21 CFR 872.6640 in the Dental (DE) specialty.

510(k) Clearances

17 matches
K Number
Device Name
IMTEC BONE COLLECTOR SYSTEM
TAP EXPRESS EJECTOR
SUPER EVACRETRACTOR, DISPOSABLE ORAL EVACUATOR
OROSCOPE MODEL NUMBER COS-100
DENTAL SANI-SLEEVE STERILE 60MM X 1650MM #1101
DENTAL SANI-SLEEVE STERILE 100MM X 2200MM #1102
DRI-CLAVE LIQUID KLEENZALL
PORTABLE FIELD DENTAL OPERATING & TREATMENT UNIT
TITANIUM SUCTION TIP
VAC - RITE RIGHT ANGLE ASPIRATOR TUBE & HOLDER
EVACUATOR TIPS
SPACELINE HIGH VOLUME EVACUATION HANDPIE
MVS UNIT, MODEL SEU-8 AND DEU-8, 80
MVS-MODEL SEU-6, DEU-6
STERI-VAC POWER UNITS
DENTAL OFFICE ENVIRONMENT CONTROL UNIT
AUTO-RINSE

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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