510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K100213Substantially Equivalent

Lumanosity Celebrity, Model 204

Lumanosity, Inc., Studio City CA / Traditional, Substantially Equivalent

K100213 is the FDA 510(k) clearance record for LUMANOSITY CELEBRITY, MODEL 204, a class II device, cleared for Lumanosity, Inc. on under FDA product code ILY (Lamp, Infrared, Therapeutic Heating). FDA records list one 510(k) clearance for Lumanosity, Inc. As of , FDA records show no recalls naming K100213.

Clearance record

Decision date
Received
(252 days to decision)
Product code
ILY Lamp, Infrared, Therapeutic Heating
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Applicant
Lumanosity, Inc. 11271 Ventura Blvd., Studio City CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ILY

Trailing 12 months
1 clearance under product code ILY in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code ILY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260