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: ELL FDA class 2

Teeth, Porcelain

Dental

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Porcelain Teeth are high-fired ceramic artificial teeth used in the construction of complete and partial dentures, valued for their excellent aesthetic properties, color stability, hardness, and resistance to staining compared to acrylic resin alternatives. They are classified as FDA Class 2 (moderate risk), requiring 510(k) premarket clearance. The product code is ELL, regulated under 21 CFR 872.3920 in the Dental (DE) specialty. This device is eligible for third-party review.

510(k) Clearances

39 matches
K Number
Device Name
Additive Manufacturing Zirconia Customized Restoration
Franz Zirconia Dental Crown
NobelProcera HT ML FCZ Bridge
NobelProcera HT ML Full Contour Zirconia Crown
PROCERA BRIDGE ZIRCONIA 9 UNITS-14 UNITS, MODELS 30-4004 TO 30-4013
SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.
PROCERA BRIDGE ZIRCONIA
PROCEARA COPINGS AND PONTIC
ARGI-SATIN OR OPTI0-STAR
MATCHMAKER/PROPAQUE PORCELAIN
IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013
VIVOPERL-PE, VIVAPERL-PE ORTHOTYP/ORTHOTYP A
DUCERAGOLD, DUCERATIN
CAPS
MICRODOSE PORCELAIN ETCHANT
MICRODOSE SILANE
IPS CERAMIC ETCHING GEL
4% ACIDULATED PHOSPHATE FLUORIDE ETCHING GEL
TYCERAMIC
SYSNPAR PORCELAIN
PROCERAM PORCELAIN
DEN-MAT LAMI-QUICK
TUF-COAT
CRYSTAR(TM) ANTI-GREENING LIQUID
CRYSTAR(TM) VINTAGE PORCELAIN
SPECTRUM
G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER
DEN-MAT PORETCH (PORCELAIN ETCHANT)
DUCERAM-METAL-CERAMIC DENTAL PORCELAIN SYSTEM
MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN
ARTIFICIAL TEETH, PORCELAIN, MODIFIED
DENTAL PORCELAIN-VARIOUS
CAPA PRE-FORMED PORCELAIN CROWN
NATURA-DENT VACUUM-FIRED PORCELAIN TEETH
THERMOCRAFT PORCELAIN
PORCELAIN ARTIFICIAL TEETH
MYERSON R&KENSON R PORCELAIN ANT&POS.-
NU-GLAZE
BIOBOND MASTER STAIN AND GLAZE 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.

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