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: LWH FDA class 1

Counter, Sponge, Surgical

General Hospital

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The Surgical Sponge Counter (product code LWH) is a device used during surgical procedures to track and count sponges and other surgical materials to prevent inadvertent retention of foreign objects in the patient. Regulated under 21 CFR 880.2740 and classified as a Class 1 device subject only to general controls, it is reviewed under the General Hospital panel within the General Hospital specialty. It is not an implant, is not life-sustaining, and is not GMP-exempt.

510(k) Clearances

15 matches
K Number
Device Name
PIXEL APP
PIXEL APP
ORLOCATE SYSTEM MODEL ORL 100
SMARTWAND-DTX
SMARTSPONGE PLUS SYSTEM
SMARTSPONGE SYSTEM
MEDLINE SURGICAL SPONGE SCANNER
RF SURGICAL SYSTEMS INC. DETECTION SYSTEM, MODEL 100A
SURGICOUNT SAFETY-SPONGE SYSTEM
MARKWELL GAUZE SPONGE
POCKET COUNT OR SAFETCOUNT
SPONGE COUNT
DEVON SPONGE COUNTER BAGS
GORSK SPONGE CONTAINMENT SYSTEM
SPONGE COUNTER

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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