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: EXB FDA class 1

Collector, Ostomy

Gastroenterology, Urology

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The ostomy collector is a pouching or collecting system worn over a surgically created stoma to collect intestinal or urinary output following procedures such as colostomy, ileostomy, or urostomy. It is classified as FDA Class 1, indicating minimal risk, subject only to general controls. The product code is EXB, regulated under 21 CFR 876.5900 in the Gastroenterology, Urology specialty. No implant, life-sustaining, GMP-exempt, or third-party review designations apply.

510(k) Clearances

50+ matches
K Number
Device Name
SmartBag (SmartPouch)
OSTOM-I ALERT
LAKE OSTOMY CARE SET
ODOR-END EMERGENCY CLEAN UP POWDER
CONSEAL COLOSTOMY CONTINENCE SYSTEM (ONE-PIECE)
EMERGENCY-CLEAN UP(TM) ECP
COMBINATION NITE DRAINAGE UNIT
'CATCH-IT' OR FECAL CONTAINMENT DEVICE
ODOR-SAFE(TM)(LIQUID) ODOR-SAFE(TM) POWDER
OSTO-PURE
PALEX (R) OSTOMY
E-Z LOOP
EZ TAC FILTER
PERSONAL PUNCH
ULTRA-GEL - #4083
BARD IRYFIX(TM) STOMA CAP
COLOPLAST CONVEX RING
DURAHESIVE PROTECTIVE BARRIER WIPE
MEDI-WIPES UNITED ANTISEPTIC SKIN PREP
DURAHESIVE WAFER WITH FLANGE
CONFIDENT ODOR ELIMINATOR
OSTOMY BAGS URETHEROSTOMY
OSTOMY BAGS COLOSTOMY
OSTOMY BAGS ILEOSTOMY
STOMAHESIVE SKIN BARRIER STERILE
JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT
DISPOSABLE UROSTOMY POUCH
BARD PERISTOMAL PASTE
DISPOS. DRAINABEL POUCH FOR ILEOSTOMY/COLOSTOMY
UNITED SKIN BARRIERS
COLOPLAST URO 2002 UROSTOMY SYSTEM
JOHNSON & JOHN SON OSTOMY PASTE PROTECTIVWE SKIN
UNITED SKIN BARRIERS
SUR-FIT IRRIGATION ADAPTER FACEPLATE
OSTOMY OR UROSTOMY ABDOMINAL BELT OS
OSTOMY FREEDOM KIT
SWEEN-A-PEEL PERISTOMAL WAFERS
ACTIVE LIFE ONE-PIECE CLOSED-END POUCH
ACTIVE LIFE ONE-PIECE STOMA CAP
COMFEEL PROTECTIVE FILM
BANGORT LIFESTYLE COLOSTOMY POUCHES
MC 2002 OSTOMY POUCHES & SKIN FLANGES
MC 2000 OSTOMY POUCHES
FILTRODER FILTERS
SUR-FIT UROSTOMY POUCH W/ACCUSEAL
BARD KARAYA GUM WASHERS
STERILE DRAINAGE SYSTEM
COMFEEL PASTE
COMFEEL BARRIER CREAM
COMFEEL CLEANSER

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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