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: GAL FDA class 2

Suture, Absorbable, Natural

General, Plastic Surgery

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The Suture, Absorbable, Natural (product code GAL) is a surgical suture made from natural materials that degrades and is absorbed by the body during the healing process, used for closing wounds and approximating tissue in general and plastic surgery. It is classified as FDA Class 2, which requires a 510(k) premarket notification to demonstrate substantial equivalence. The device is regulated under 21 CFR 878.4830 in the General, Plastic Surgery specialty (SU). This device carries an implant designation, as it is embedded within body tissue at the time of application.

510(k) Clearances

30 matches
K Number
Device Name
Surgical Gut Suture
DEMETECH ABSORBABLE SURGICAL SUTURE PLAIN & CHROMIC GUT
UNIPLAIN & UNICHROM
AUTOBAHN TISSUE CLOSURE DEVICE AND DISPOSABLE CARTRIDGE
SUTURTEK FASTCLOSE SUTURING DEVICE
SERRALGUT
GRAMS ABSORBABLE SURGICAL GUT SUTURE PLAIN & CHROMIC
SUTURTEK FASTCLOSE FASCIA CLOSURE DEVICE
PLAIN AND CHROMIC GUT ABSORBABLE SURGICAL SUTURES USP
PLAIN AND CHRONIC GUT ABSORBABLE SURGICAL SUTURES, USP
LIGA-LOOP SUTURE APPLICATOR
PLAIN/CHROMIC CATGUT
AILEE SUTURES AND AILEE NEEDLES
ABSORBABLE SURGICAL GUT SUTURE, PLAIN AND CHRONIC AND SOFTCAT ABSORBABLE SURGICAL GUT SUTURE, PLAIN AND CHRONIC
PLAIN GUT & CHRONIC GUT ABSORBABLE SURGICAL SUTURES USP
CHROMIC CATGUT
PLAIN CATGUT
SURGICAL SUTURES, PGL, GUT, DEKLENE, OPTHAMEND ETC
SURGICAL SUTURE PACKAGE INSERTS
CATGUT SUTURE CHROMIC
CATGUT SUTURE PLAIN
REVISED LABELING FOR CHROMIC AND PLAIN GUT SUTURES
PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR
LUKENS SURGICAL GUT SUTURE
STERILE PLAIN GUT/CHROMIC GUT ABSORB SURG SUTURES
AUTO SUTURE(R) MODIFIED ENDOSCOPIC LIGATING LOOP
PLAIN AND CHROMIC GUT SUTURE
ENDOSCOPIC HEMOSTATIC LIGATING LOOP
GUT SUTURES
ABSORBABLE SURGICAL GUT SUTURE*

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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