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: EWL FDA class 2

Prosthesis, Laryngeal (Taub)

Ear, Nose, Throat

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The Taub laryngeal prosthesis is a device designed to restore voice function in patients following laryngectomy or laryngeal surgery by providing a means for the passage of air from the trachea to the pharynx to generate speech. It is classified as FDA Class 2, representing moderate risk, and requires 510(k) premarket clearance. The product code is EWL, regulated under 21 CFR 874.3730 in the Ear, Nose, Throat specialty. No special implant, life-sustaining, or GMP-exempt flags apply.

510(k) Clearances

40 matches
K Number
Device Name
FirstFit Surgical Kit
PROVOX FREEHANDS FLEXIVOICE
PROVOX VEGA PUNCTURE SET
PROVOX ACTIVALVE (SIZE 4.5MM, 6MM, 8MM, 10MM, 12.5MM)
BLOM-SINGER INDWELLING TEP OCCLUDER
PROVOX VEGA, MODEL 8130-8135
BLOM-SINGER DUAL VALVE INDWELLING VOICE PROSTHESIS, MODELS DV-1600 SERIES, DV-2000 SERIES
PROVOX NID VOICE REHABILITATION SYSTEM, MODEL REF 7101 TO 7134
PROVOX FREEHANDS HME, MODEL 7710
BLOM-SINGER INDWELLING 2000 VOICE PROSTHESIS
VOICE MASTER PROSTHESIS
PROVOX 2 VOICE PROSTHESIS SYSTEM
INHEALTH BLOM-SINGER INDWELLING VALVED INSERT ACCESSORY DEVICE
INHEALTH BLOM-SINGER INDWELLING PLUG INSERT ACCESSORY DEVICE
PROVOX(TM) VOICE PROSTHESIS
BLOM-SINGER INDWELLING LOW PRESSURE VOICE PROSTHES
BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET
BLOM-SINGER LOW PRESSURE VOICE PROSTHESIS,P.I.D.S.
BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET
SINGH SPEECH SYSTEM (SERIES 'SSS')
BIVONA-COLORADO VOICE PROSTHESIS
BLOM-SINGER SHOWER GUARD
BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT
BLOM-SINGER(R) TRACHEOESOPHAGEAL PUNCTURE KIT
BIVONA ULTRA LOW RESISTANCE VOICE PROSTHESIS
ESKA-HERRMANN TRACHEOSTOMY VALVE
BIVONA ECONOMY DUCKBILL VOICE PROSTHESIS
DACOMED CORP. ESKA-HERRMAN VOICE PROSTHESIS
FLEXIBLE GRASPING FORCEPS
THE GRONINGEN VOICE PROSTHESIS
BLOM-SINGER LOW PRESSURE VOICE PROSTHES
DUCKBILL VOICE PROSTHESIS & TRACHEO
BLAISE-RATHAEL VOICE PROSTHESIS
LOW PRESSURE BLOM-SINGER VOICE PROSTHES
BLOW-SINGER TRACHEOSTOMA VALVE
PERISCOPE VOICE PROSTHESIS
BLOM-SINGER VOICE PROSTHESIS
SILASTIC VOICE PROSTHESIS
PANJE VOICE PROSTHESIS
BLOM-SINGER DUCKBILL VOICE PROSTHESIS

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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