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: FDI FDA class 2

Snare, Flexible

Gastroenterology, Urology

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The Flexible Snare (product code FDI) is an electrosurgical accessory consisting of a flexible wire loop passed through an endoscope to encircle and resect polyps or other lesions in the gastrointestinal or urological tract. It is an FDA Class 2 device (moderate risk), requiring 510(k) premarket clearance. It is regulated under 21 CFR 876.4300 in the Gastroenterology and Urology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Polypectomy Snare
CORE-SNARE
Disposable Polyp Snare
Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare
Disposable Polypectomy Snare
SmartBand EMR Kit (SB-EMR-K, SB-EMR-K-12, SB-EMR-K-9.4), SmartBand EMR Pack (SB-EMR-P, SB-EMR-P-12, SB-EMR-P-9.4), SmartSnare EMR Hexagonal Snare (SS-230-1 or packaged with kit)
Captivator Single-Use Polypectomy Snares, Captiflex Single-Use Polypectomy Snares
Lariat, Hot/Cold Snare
SmartBand EMR Kit, SmartBand EMR Pack, SmartSnare
AcuSnare Polypectomy Snare - Duckbill
ClearGrasp Snare
Roth Net Retriever Product Line
AcuSnare Polypectomy Snare
Polypectomy Snare
Rotatable Snares, Non-Rotatable Snares
Single Use Electrosurgical Snare SD-400
Rotatable Snares
rescuenet
Polypectomy Snare
Lariat snare
TRACTION POLYPECTOMY SNARE
PolyCatch Retrieval Device
CAPTIVATOR EMR DEVICE FOR STANDARD GASTROSCOPES - BOX 1, CAPTIVATOR EMR DEVICE FOR STANDARD GASTROSCOPES - BOX 5, CAPTIV
MONOFILAMENT POLYPECTOMY SNARE
CAPTIVATOR II,SINGLE-USE POLYPECTOMY SNARES
MULTI-STAGE SNARE
SENSATION SHORT THROW, CAPTIFLEX, CAPTIVATOR, CAPTIVATOR II, PROFILE, SINGLE-USE POLYPECTOMY SNARES
EC SINGLE USE, POLYPECTOMY SNARE
ROTH NET RETRIEVER
UROLOGY MONOPOLAR SNARE FOR TISSUE TRANSECTION
DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998
TORNADO ROTATABEL SNARE AND POLYP CATCHER
ETHICON ENDO SURGERY ARTICULATING SNARE
COOK IRELAND SONNET POLYPECTOMY SNARE
INJECTOR NEEDLE/SNARE
HORIZONS REUSABLE POLYPECTOMY SNARES
NAKAO SNARE II AND NAKAO SNARE III
HORIZONS INTERNATIONAL POLYPECTOMY SNARES
SNARE,FLEXIBLE
ROTOSNARE
MILL-ROSE DISPOSABLE POLYPECTOMY SNARE
IRRIGATION/ASPIRATION POLYPECTOMY
SNARE
OLYMPUS SD SERIES SNARES
MILL-ROSE ROTATABLE POLYPECTOMY SNARE
GIP/MEDI-GLOBE POLYPECTOMY SNARES
SNARE, FLEXIBLE, ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES
PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES
INJECT-SNARE
AMERICAN CATHETER POLY-SNARE

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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