Medi Lift PLUS— 510(k) K220198

Substantially Equivalent

Ya-Man, Ltd.

FDA 510(k) clearance K220198 for Medi Lift PLUS, Substantially Equivalent on 2023-06-28. 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: 2022-01-24
Decision date: 2023-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Koto-Ku, JP

Download summary PDF View on FDA.gov ↗

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K260895 — Ulike Clear Zero (YC10 BU)2026-05-28

More clearances from Ya-Man, Ltd.

K250618 — Medi Lift Essential Eye Mask2025-10-29
K244048 — Medi Lift Mask2025-01-16
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.