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: KGE FDA class 2

Forceps, Biopsy, Electric

Gastroenterology, Urology

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Electric Biopsy Forceps are endoscopic instruments that combine mechanical grasping with electrosurgical energy to obtain tissue samples and simultaneously coagulate the biopsy site, used in urological or gastroenterological endoscopic procedures to minimize bleeding during tissue sampling. It is classified as FDA Class 2, indicating moderate risk; devices in this category are subject to general controls and special controls, and typically require 510(k) premarket notification demonstrating substantial equivalence to a predicate device. The product code is KGE, regulated under 21 CFR 876.4300, within the Gastroenterology, Urology medical specialty. This device is eligible for third-party review.

510(k) Clearances

44 matches
K Number
Device Name
ClearHemograsper
Disposable Hot Biopsy Forceps
Diathermic Slitter (FlushKnife) DK2620JI and DK2623JI
Bipolar Coagulation Foreceps
Ensure Single-Use Coagulation Forceps
Avulsion Forceps
Disposable Hot Biopsy Forceps
Ensizor Monopolar Endoscopic Scissors
Captura® Disposable Hot Biopsy Forceps
Single Use Hot Biopsy Forceps FD-231
Fujifilm Diathermic Slitter (FlushKnife)
Fujifilm Diathermic Slitter (FlushKnife), Fujifilm Diathermic Slitter (ClutchCutter)
Disposable Hot Biopsy Forceps
Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)
ENDO-MARYLAND DISSECTOR
ENDOCHOICE HOT BIOPSY FORCEPS
RADIAL 4 HOT BIOPSY FORCEPS BOX 5; RADIAL JAW 4 HOT BIOPSY FORCEPS BOX 20; RADIAL JAW 4 HOT BIOPSY FORCEPS BOX 40
MULTI-BITE HOT BIOPSY FORCEPS
ENDOSCOPIC MONOPOLAR SCISSORS, MODELS EMS-235, EMS-165
ELECTROSURGICAL HEMOSTATIC FORCEPS SERIES
REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS
HORIZONS REUSABLE HOT BIOPSY FORCEPS
HORIZONS HOT BIOPSY FORCEPS
WILSON-COOK REUSABLE HOT BIOPSY FORCEPS
HOT BIOPSY FORCEPS FEENESTRATED 230 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATED 160 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATD
WILTEK HOT BIOPSY FORCEPS
UNIPOLAR OPTICAL BIOPSY FORCEPS
RESUABLE HOT BIOPSY FORCEPS
DYNABITE HOT GI BIOPSY FORCEPS
LSVP INTERNATIONAL HOT BIOPSY FORCEPS
GIP/MEID-GLOBE HOT BIOPSY FORCEPS
OLYMPUS FD-1/2-1 HOT BIOPSY FORCEPS
OLYMPUS FD-5 HOT BIOPSY FORCEPS
KARL STORZ INSULATED BIOPSY FORCEPS, GRASPING/DISSECTING FORECPS, FLEXIBLE FORCEPS
HOT BIOPSY FORCEPS
BASICS ENDOSCOPY SYSTEM
SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN
THERMAL OPTION
DISPOSABLE HOT BIOPSY FORCEPS
BIOPSY FORCEPS, ELECTRIC
HOT BIOPSY FORCEPS
HOT BIOPSY FORCEPS
BIPOLAR BIOPSY FORCEPS
PORGES HOT BIOPSY FORCEPS

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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