Medi Lift Mask— 510(k) K244048

Substantially Equivalent

Ya-Man, Ltd.

FDA 510(k) clearance K244048 for Medi Lift Mask, Substantially Equivalent on 2025-01-16. Applicant: Ya-Man, Ltd.. Device class: 2.

Clearance details

Applicant: Ya-Man, Ltd.
Product code: Code NFO
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2024-12-31
Decision date: 2025-01-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Tokyo, JP

Download summary PDF View on FDA.gov ↗

Recent devices under product code NFO

K262861 — PureLift Pro Max2026-09-11
K260387 — SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)2026-08-31
K253932 — FACEGYM Pro Device (HD-109)2026-07-23
K260179 — VITA Multi-Function Head Brush (TB-2343F, TB-2442F)2026-06-03
K260895 — Ulike Clear Zero (YC10 BU)2026-05-28

More clearances from Ya-Man, Ltd.

K250618 — Medi Lift Essential Eye Mask2025-10-29
K220198 — Medi Lift PLUS2023-06-28
K112016 — L-SER KO LAMP2012-02-10
K032944 — YA-MAN LASER 212003-12-19
K011021 — LASER 202001-10-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.