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: PBX FDA class 2

Massager, Vacuum, Radio Frequency Induced Heat

General, Plastic Surgery

View full classification →

The Massager, Vacuum, Radio Frequency Induced Heat is a combination device that uses vacuum massage and radiofrequency-induced heat to generate warmth in body tissues for minor relief of aches and pain, and to provide a temporary reduction in the appearance of cellulite. It falls under the General and Plastic Surgery medical specialty and is classified as a Class 2 device under regulation 878.4400, requiring 510(k) premarket notification. The device is eligible for third-party review. It is not an implant and is not life-sustaining.

510(k) Clearances

50+ matches
K Number
Device Name
Zionic Pro Max (Radiofrequency)
HEBE (NP0000763)
Préime DermaFacial Collagen+
XOD Diathermia Radiofrequency Device
Indiba Diathermia Radiofrequency Deep Care Device (Deep care IDC0409/EVONY ); Indiba Diathermia Radiofrequency Activ Device (Activ ACT0309/CT9)
FISIOWARM 7.0
MIRARI® Cold Plasma System ( GV-M2-01)
INDIBA COMPACT devices
DEFINE System (AG612444A)
eMVFit (MVF-10M)
RFG-01
NuEra Tight RF Model OptiStream
BACK 3
Zionic Aesthetic
ThermoTK
NuEra Tight RF Model APMD145.M70-US
Symmed Elite Aesthetic
Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500
RSHOCK
Doctor Tecar Plus, Doctor Tecar Smart
C.C. LIFE 21
Back 3 COLOR
Palm NRG cellulite body device (model: Palm NRG body device)
Apollo Duet (Model : APD-4000)
Diacare 7000
Venus BlissMAX
Venus BlissMAX
Deka Tiac II
Family of Venus RF Systems - Venus Freedom
Sectum
RF Thermal System
Evolve System with the T3 Applicator
NuEra Tight RF, NuEra Tight RF Plus
V30 system, V20 system, V10 system, V-VR Hand piece
Palm NRG cellulite and muscle toning body device
Ultimate Contour, Ultimate Contour Mini
NuEra Tight, NuEra Tight EMS
V30 System, V20 System, V10 System, V-FR Handpiece
V30 system, V20 system, V10 system, V-FC Handpiece
TempSure System
CAPENERGY - C100, C200, C300, C400, C50
Deka Tiac 1
EmFace Device
Venus Bliss
EmBody System
BTL-084
Doctor Tecar
Family of Venus RF Systems - Heal
T-PLUS
Human Tecar HCR 1002

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.

Popular Product Codes

Commonly searched