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: EIS FDA class 1

Remover, Crown

Dental

View full classification →

The Crown Remover is a dental instrument used to dislodge and remove cemented or temporarily attached dental crowns from prepared tooth abutments without damaging the crown or the underlying tooth structure. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is EIS, regulated under 21 CFR 872.4565 in the Dental (DE) specialty.

510(k) Clearances

19 matches
K Number
Device Name
ATD AUTOMATIC BRIDGE REMOVER
EASY PNEUMATIC CROWN AND BRIDGE REMOVER
STAINLESS STEEL DEN. CROWN REMOVER & AMA./COMP.CAR
HAZELTON TEMPORARY CROWN AND BRIDGE REMOVER
H-TYPE BRIDGE REMOVER
C & B 40 PENTRO C & B40
SATIN CAST ECONOCAST
C & B 45
C & B 61 PENTRON C & B61
GOLD-PALLADIUM-SILVER BASED CAST/ALLOY
SUPRA AP CHOICE 83
RX IV PENTRON IV
C & B57 PENTRON C & B57
RX NYSP PENTRON 60
NATURELLE-LITE
RX 41 PENTRON 41
RX D PENTRON
RX SEG ECONOPLUS
RX ORY PENTRON C & B

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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