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: ELR FDA class 1

Post, Root Canal

Dental

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The Root Canal Post is a dental component inserted and cemented into the prepared root canal space following endodontic treatment, providing structural retention for a core build-up and overlying crown in teeth with insufficient coronal tooth structure. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is ELR, regulated under 21 CFR 872.3810 in the Dental (DE) specialty.

510(k) Clearances

35 matches
K Number
Device Name
FIBER-METAL POST
FRC POSTEC PLUS
EVERSTICK POST
FIBIOCORE
CARBON POST
FRC POSTEC
GLASS POST
SNOWPOST, SNOWLIGHT
HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST
HARALD NORDIN CARBONITE CARBON FIBER COMPOSITE DENTAL POST
TENAX WHITE POST
PARAPOST FIBER WHITE
FIBREKOR POST SYSTEM
KURER CROWN SAVER K4 ANCHOR SYSTEM-THE UNIVERSAL KIT, KURER STANDARD K4 ANCHOR SYSTEM- THE READY CORE KIT, KURER FIN-LOC
BIO-POST DENTAL POST SYSTEM
COSMOPOST
C-POST
THE STERN ROOT ANCHOR SYSTEM
INTEGRAPOST
CONSERVA POST SYSTEM
PARAPOST XT SYSTEM
THERMAPOST ENDODONTIC ROOT CANAL POST
DENTAL SCREW POSTS
VERSADOWEL POST SYSTEM
ENDODONTIC POST W/ ACCESSORIES
PDI PARALLEL SIDED POST KIT
ENDO-CORE
FILPOST
FLEXI-CAST CROWN CORE SYSTEM
AD POST
CENTRIX TRI-LAMINATE POST SYSTEM
DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM
ARCEE DENTAL POST
BETA POST
ROOT CANAL POST

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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