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: GDL FDA class 1

Needle, Suturing, Reusable

General, Plastic Surgery

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The Needle, Suturing, Reusable (product code GDL) is a reusable surgical needle designed to pass suture material through tissue for wound closure or tissue approximation in general and plastic surgery, intended to be sterilized and used across multiple procedures. It is classified as FDA Class 1, the lowest risk category, subject only to general controls and not requiring premarket notification. The device is regulated under 21 CFR 878.4800 in the General, Plastic Surgery specialty (SU). No special flags apply to this device.

510(k) Clearances

5 matches
K Number
Device Name
NON-STERILE SUTURE NEEDLES
25-420 TO 25-436 VARIOUS TYPES OF SUTURE NEEDLES
25-450 TO 25-540 VARIOUS SUTURE FORCEPS
SHARTPOINT EYED NEEDLES
UNIVERSAL SUTURE PASSER

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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