Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K112016Substantially Equivalent

L-Ser Ko Lamp

YA-Man Ltd., Richmond VA / Traditional, Substantially Equivalent

K112016 is the FDA 510(k) clearance record for L-SER KO LAMP, a class II device, cleared for Ya-Man, Ltd. on under FDA product code ILY (Lamp, Infrared, Therapeutic Heating). FDA records list 6 510(k) clearances for Ya-Man, Ltd., from to . As of , FDA records show no recalls naming K112016.

Clearance record

Decision date
Received
(211 days to decision)
Product code
ILY Lamp, Infrared, Therapeutic Heating
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Applicant
Ya-Man, Ltd. 9210 Forest Hill Ave., Richmond VA
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