ClearanceBrief
Company ยท US

Ya-Man, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2025. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NFOStimulator, Transcutaneous Electrical, Aesthetic Purposes3
GEXPowered Laser Surgical Instrument2
ILYLamp, Infrared, Therapeutic Heating1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 29, 2025K250618Medi Lift Essential Eye Mask
Ya-Man, Ltd., JP
NFO
Jan 16, 2025K244048Medi Lift Mask
Ya-Man, Ltd., JP
NFO
Jun 28, 2023K220198Medi Lift PLUS
Ya-Man, Ltd., JP
NFO
Feb 10, 2012K112016L-SER KO LAMP
Ya-Man, Ltd.
ILY
Dec 19, 2003K032944YA-MAN LASER 21
Ya-Man, Ltd.
GEX
Oct 9, 2001K011021LASER 20
Ya-Man, Ltd.
GEX

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes