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: EKM FDA class 1

Gutta-Percha

Dental

View full classification →

Gutta-Percha is a natural thermoplastic polymer derived from tropical trees, formed into standardized cones or points and used as the primary material to obturate (fill and seal) prepared root canals following endodontic treatment. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is EKM, regulated under 21 CFR 872.3850 in the Dental (DE) specialty.

510(k) Clearances

23 matches
K Number
Device Name
EI DOWNPAK BARRIER SLEEVES
DOWN PAK
TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)
ENDO TWINN
FIBERFILL SGP
ANTIBACTERIAL GUTTA PERCHA
THERMAPREP PLUS OVEN
INJECT-R FILL
MICRODOSE RC-EZ
TOUCH 'N HEAT MODEL 5002, MODIFICATION
THERMAPREP
THERMAFIL ENDODONTIC OBTURATOR
ENDO-PREP
THERMAFIL ENDODONTIC OBTURATOR
GUTTA PERCHA
GUTTA PERCHA POINTS
SET CANAL SEALER PASTE
ULTRAFIL-LT (GUTTA PERCHA)
HEATED GUTTA PERCHA DELIVERY SYSTEM
GUTTA PERCHA POINTS
PAPER POINTS
TOUCH-N-HEAT MODEL 5001
OBTURATION SYSTEM KIT

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.

Popular Product Codes

Commonly searched