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: EIC FDA class 1

Syringe, Periodontic, Endodontic, Irrigating

Dental

View full classification →

The Periodontic and Endodontic Irrigating Syringe is a specialized dental syringe used to deliver irrigating solutions into the periodontal sulcus or root canal during periodontal and endodontic treatments, removing debris and reducing bacterial load. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is EIC, regulated under 21 CFR 872.4565 in the Dental (DE) specialty.

510(k) Clearances

16 matches
K Number
Device Name
RCT GEL ROOT CANAL THERAPY GEL
MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)
HYDRON ROOT CANAL FILLING & MARK IV STARTER KIT
MAX-I-PROBE HANDPIECE
MAX-I-PROBE PERIODONTAL ENDODONTIC PROB
R & S SERIES FITTING TOOLS
WATER PISTOL
ROOT CANAL FILLING APPLICATOR NEEDLES
MARK IV SYRINGE
ENDOVAGE SYRINGE
EPIC CANNULA
CENTRIX MKIV ENDODONTIC DELIVERY
GUTTA GUN
SYRINGE, ENDODONTIC, W/PERFORATED NEEDLE
ENDOGATOR
SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE

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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