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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

Free to try · every answer cites its records

Product Code: GDY FDA class 1

Gauze/Sponge, Internal, X-Ray Detectable

General, Plastic Surgery

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The Gauze/Sponge, Internal, X-Ray Detectable (product code GDY) is a surgical gauze or sponge used inside the body during procedures to absorb blood and fluids, featuring radiopaque material that makes it detectable by X-ray to prevent accidental retention within the patient after surgery. It is classified as FDA Class 1, posing minimal risk, subject only to general controls and not requiring premarket notification. The device is regulated under 21 CFR 878.4450 in the General, Plastic Surgery specialty (SU). No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
ULTRACELL SUCTION SPONGE
CPR LAP SPONGES
STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE
PROTEC X-RAY DETECTABLE GAUZE SPONGE
KENSORB
TRIANGULAR SPONGES
ROSEBUD DISSECTOR
KITTNER DISSECTOR
ROUND STICK SPONGES, FLAT STICK SPONGES
CHERRY PIT DISSECTOR
CHERRY DISSECTOR
CYLINDRICAL SPONGE
GAUZE, NONABSORABABLE, X-RAY DETECTABLE (INTERNAL SPONGE)
ULTRACELL ORTHOPEDIC SPONGES
ULTRACELL ORTHOPEDIC SPONGES
ULTRACELL ORTHOPEDIC SPONGES
ULTRACELL RETRACTOR COVERS
ROUND STICK SPONGES, FLAT STICK SPONGES
CYLINDRICAL SPONGE
KITTNER DISSECTOR
TRIANGULAR SPONGES
CHERRY DISSECTOR
GAUZE SPONGES
OREX
OREX (12X12 X-RAY DETECTABLE)
OREX (18X18 X-RAY DETECTABLE)
CHERRY PIT DISSECTOR
ROSEBUD DISSECTOR
PEANUT DISSECTOR
SPONGE, LAPAROTOMY, VARIOUS SIZE
LORREX GAUZE SPONGES, X-RAY DETECTABLE
STERILE X-RAY DETECTABLE GAUZE SPONGES
LAP SPONGE PRODUCT LINE
ISOLYSER (18X18 X-RAY DETECTABLE)
ISOLYSER (4X18) X-RAY DETECTABLE
ISOLYSER (8X4 12 PLY X-RAY DETECTABLE)
ISOLYSER (X-RAY DETECTABLE)
DUPAQUE SPONGE
STERILE LAPAROTOMY SPONGES
NEUROLOGICAL SPONGES
SURGICAL SPONGE X-RAY DETECTABLE
X-RAY PACKING SPONGE
SPECIALTY SPONGES
TONSIL SPONGES
TENCEL X-RAY DETECTABLE SPONGES/LAP PADS
STERILE GAUZE SPONGES X-RAY DETECTABLE
SURGICAL SPONGES
SPECIALTY SPONGES
LAP SPONGES, MODIFIED
DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED

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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