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: NFO FDA class 2

Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Neurology

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The Stimulator, Transcutaneous Electrical, Aesthetic Purposes (product code NFO) is a neurology device that applies transcutaneous electrical stimulation to facial or body muscles for aesthetic purposes such as skin tightening or muscle toning, distinct from therapeutic TENS devices. It is classified as an FDA Class 2 device within the Neurology specialty, requiring 510(k) premarket clearance. No specific regulation number has been assigned to this product code. The device is not flagged as an implant or life-sustaining device.

510(k) Clearances

50+ matches
K Number
Device Name
VITA Multi-Function Head Brush (TB-2343F, TB-2442F)
Ulike Clear Zero (YC10 BU)
DeepSkin (DEP100)
Aura Glide (FC40)
Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003 SKB-2109,SKB-2129,SKB-2208PRO, SKB-2209)
Medi Lift Essential Eye Mask
JOVS Electric Stimulation Beauty Device (JE2)
Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)
Facial & Body Beauty Device (INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507)
Sunny Plus (Sunny)
NeurotriS (SX2500); NeurotriS (SX3800)
MF SC GEN2 Facial Toning System
Microcurrent Facial Device (CEC101, EE0101, EEI101)
SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1
Préime DermaFacial (MicroT)
PureLift GLOW
Myolight Microcurrent Handpiece
JMOON NouvelleSkin Facial Toning Device (M30U PR, M30U MW, M30U SG, M30U SK, M30U MP)
Medi Lift Mask
Micro-current Facial Beauty Device (AM-810B, AM-810W, AM-812B, AM-812W)
BTL-785BNF-E
NuFACE® FIX+
BEAR 2 Body
Facial Toning device (UIC-189); Facial Toning device (UIC-589)
MF SC Facial Toning System
Nu Skin RenuSpa iO
Beagank 4T Plus
C.C. Life 21
BTL-785BNF Handpiece
Medi Lift PLUS
PureLift Pro Edition
Myolift QT
PureLift Pro Plus
Luminice
Microcurrent device (Model: HBR2-1)
TheraFace Microcurrent
ZIIP+ Device
Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device
Trinity ELE Plus and Trinity ELE Plus Pro
NuFACE Mini Plus
NuFace Trinity Plus Device
Tua Face Fitness / Tua Trend Face
BEAR and BEAR mini
NuFACE Mini Device
PureLift
Ultra OTC Facial Toning System
NuFACE FIX Skin Toning Device
NuFACE Trinity
Ultra Facial Toning System
TAMA BEMS device

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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