Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K860159Substantially Equivalent

Thumper (Vibrator/massager)

Wellness Innovations Corp., Canada L3r 4b5, CA / Traditional, Substantially Equivalent

K860159 is the FDA 510(k) clearance record for THUMPER (VIBRATOR/MASSAGER), a class I device, cleared for Wellness Innovations Corp. on under FDA product code IRO (Vibrator, Therapeutic). FDA records list one 510(k) clearance for Wellness Innovations Corp. As of , FDA records show no recalls naming K860159.

Clearance record

Decision date
Received
(21 days to decision)
Product code
IRO Vibrator, Therapeutic
Regulation
21 CFR 890.5975
Device class
Class I
Review panel
Physical Medicine
Applicant
Wellness Innovations Corp. 124 Denison St., #40, Canada L3r 4b5, CA
Third party review
No

Clearances, product code IRO

Trailing 12 months

FDA records hold no clearances under product code IRO in the trailing twelve months.

FDA records show no clearances under product code IRO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IRO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260