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: EKJ FDA class 1

Burnisher, Operative

Dental

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The Operative Burnisher is a dental hand instrument with a smooth, rounded or pear-shaped tip used to smooth and adapt the surface and margins of restorations, particularly amalgam, after placement to improve marginal seal and surface finish. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is EKJ, regulated under 21 CFR 872.4565 in the Dental (DE) specialty.

510(k) Clearances

50+ matches
K Number
Device Name
ASEPTYLUM, UNI-CARRIER
MEDTROL DENTAL KIT
DENTAL KIT
SUREFLEX FILES
INSTRUMENT,FILLING,PLASTIC,DENTAL
STAT PAK
MAUNAL DISPOSABLE DENTAL INSTRUMENTS
PRESTERILIZED ENDODONTIC FILES
SOUTHLAND STERILE DENTAL SYSTEM
NON-FOGGING DENTAL MIRROR
AMD DENTIST AND HYGIENIST KITS
EXPLORER, OPERATIVE
FORCEPS, DRESSING, DENTAL
MIRROR, MOUTH
LC DENTAL HAND INSTRUMENT
SILICONE MIRROR
APPLICATOR NOZZLE
STERILE DENTAL KITS
ECO/DENTAL GENERAL DENTAL PACK
BLUNT TIP IRRIGATION NEEDLES
PART 872 DEGUFILL H & DEGUFILL M DA
IMPLARETTE
ACCU-PLACER TM KIT
NUTIP (TM) SYRINGE SHIELD
HARDCOATED PLASTIC FILLING INSTRUMENT
PULPDENT PIC N STIC
MIRROR SHIELD
AMALGAM CONDENSER
ELEVATOR #11
U-15 SINGLE END SCALER
HAND MIRROR
DISCOID SPOON EXCAVATOR
DISCOID/CLEOID DOUBLE END AMALGAM CARVER
GRACEY CURETTE #13-14
#23 EXPLORER
5 STRAIGHT SCISSORS
PERIODONTAL KNIFE
EXPLORER 24 DENTAL HAND INSTRUMENT
DMV(R) VENEER SUCTION GRIPPER
SANI-PIKS DENTAL HAND INSTRUMENT
BREVET FLOSS PICK (AUTOCLAVE STERILIZER)
BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)
ANSWER DENTAL IMPLEMENTS, MIRROR
ANSWER DENTAL IMPLEMENT, FORCEPS
ANSWER DENTAL IMPLEMENT, EXPLORER
DENTAL HAND INSTRUMENTS
RUBBER DAM CLAMPS/FORCEPS
PRICHARD PERIOSTEAL RETRACTOR #3
MANDIBLE MANIPULATOR
DENTAL IMPRESSION SYINGE

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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