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: MIX FDA class 2

System, Vocal Cord Medialization

Ear, Nose, Throat

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The Vocal Cord Medialization System is a set of implantable devices used in laryngeal framework surgery to reposition or augment the vocal cord, improving voice quality and airway protection in patients with vocal cord paralysis or paresis. Classified as a Class 2 implantable device under 21 CFR 874.3620 within the Ear, Nose, and Throat specialty, it requires 510(k) premarket notification. It carries an implant flag, denoting its surgically placed nature.

510(k) Clearances

17 matches
K Number
Device Name
Silk Voice (SMI-04)
Silk Voice
Renu Gel
CALCIUM HYDROXYLAPATITE VOCAL FOLD IMPLANT
VF LIQUIGEL
VOCALIS AND VOCALIS SM
VOCALIS GEL
MODIFICATION TO VF GEL PLUS
VF GEL PLUS
RADIESSE LARYNGEAL IMPLANT
JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT
LARYNGEAL AUGMENTATION IMPLANT
LORENZ LACTOSORB VOCAL MEDIALIZATION IMPLANT
VOCOM SILICONE SYSTEM
VOCOM IMPLANT- 8MM
GORE REVOX THYROPLASTY IMPLANT
MONTGOMERY THYROPLASTY IMPLANT SYSTEM

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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