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: IRO FDA class 1

Vibrator, Therapeutic

Physical Medicine

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A therapeutic vibrator is an electrically powered device that applies mechanical vibration to soft tissues for therapeutic purposes such as pain relief, muscle relaxation, and improvement of local circulation. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is IRO, regulated under 21 CFR 890.5975, within the Physical Medicine medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
QI GONG MASSAGER
COMFORT, MUSCLE, CORDLESS MASSAGER, BATTERY POWERED OPERATED MASSAGER
MASSAGER THERAPUTIC, ELECTRIC
SHIATSU MASTER MASSAGER CUSHION
CHAMPION PHYSIOACOUSTICC RECLINER-TRANSPORTER CHAIR
CONAIR FAMILY FITNESS BODY ENERGY
SKALPI 3200
CONAIR BODY AND SOLE
WAHL FRESH FACE
HAND MASSAGE UNIT
CORDLESS MASSAGER WITH HEAT ( VARIOUS BRAND NAMES)
MASSAGING HELMET C.F. HANSEN DESIGN
SQUEEZE PLAY
WAHL COMPACT COMFORT MASSAGER
WAHL(R) FOOT COMFORT MASSAGER
NEXT WAVE PHYSIOACOUSTIC MATTRESS
FO96 HANDY MASSAGER
F183 AC-MINI MASSAGER WITH UL APROVED ADAPTOR
AO11 BODY MASSAGER
A013 FEMI-FORM FACIAL MASSAGER
SONASSAGE
WINDMERE MASSAGE MATE
CARAPACE SUTURE REMOVAL TRAYS
HEALTH ESSENTIALS MULTI-PURPOSE MASSAGER
HEALTH ESSENTIALS FANCY PERSONAL MASSAGER
BODYTHERM
HEALTH ESSENTIALS MAXI MASSAGER
HEALTH ESSENTIALS BODY CARE MASSAGER
HEALTLH ESSENTIALS PERSONAL MASSAGER
WINDMERE VIBRA TOUCH PERSONAL BODY MASSAGER
MINI VIBRATOR
SONIX...THERAPEUTIC SONIC MASSAGE
PAM PLUS
TOUCH N TONE 1 MASSAGER
A101 LITESSAGER
FO51/F151 GOLF MASSAGER
FO69 FANCY MASSAGER
FO92 SEATING MASSAGER
F383 RECHARGEABLE MINI MASSAGER
FO41 BODY MASSAGER
F055 B.O. FANTASTIC RELAXER
MULTI-REACH II WAND MASSAGER
SOUND RELIEF
MOTOR MASSAGE PILLOW
ULTRA WAVE 101
MINI-VIBRATOR
LEG EEZE
CHIROPRACTIC MASSAGE PILLOW
LA MASSEUSE
VASOTRAIN 447

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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