Smart Beauty Devices

Home / Companies / Ya-Man, Ltd.

Ya-Man, Ltd.

3 FDA records filed under this company name, from 2023 to 2025, in microcurrent and ems (NFO, 3).

The applicant is the company that filed with FDA. It can be the brand you know or a manufacturer that makes devices sold under other brand names; the device name as filed often shows which. We don't merge different company names, so check the A–Z list for related entries.

Electrical stimulation for aesthetic use (microcurrent and EMS) (NFO, 3)

510(k) cleared

Medi Lift Essential Eye Mask

510(k) number
K250618
Applicant
Ya-Man, Ltd.
Product code
NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation
21 CFR 882.5890, Class II
FDA decision
Substantially Equivalent (SESE)
Received

Indications for use, as filed

“The Medi Lift Essential Eye Mask is intended for facial stimulation and indicated for over-the-counter cosmetic use.”

Copied from the text of FDA's 510(k) document (PDF, page 4), with line breaks removed.

510(k) cleared

Medi Lift Mask

510(k) number
K244048
Applicant
Ya-Man, Ltd.
Product code
NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation
21 CFR 882.5890, Class II
FDA decision
Substantially Equivalent (SESE)
Received

Indications for use, as filed

“The Medi Lift Mask is intended for facial stimulation and indicated for over-the-counter cosmetic use.”

Copied from the text of FDA's 510(k) document (PDF, page 4), with line breaks removed.

510(k) cleared

Medi Lift PLUS

510(k) number
K220198
Applicant
Ya-Man, Ltd.
Product code
NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation
21 CFR 882.5890, Class II
FDA decision
Substantially Equivalent (SESE)
Received

Indications for use, as filed

“The Medi Lift PLUS is intended for facial stimulation and indicated for over-the-counter cosmetic use.”

Copied from the text of FDA's 510(k) document (PDF, page 3), with line breaks removed.