Data / Medical devices / Japan / Ya-Man Ltd.
Ya-Man Ltd.: FDA-registered device maker in Koto-ku Tokyo, Japan, 5 510(k) clearances
Ya-Man Ltd. is registered with the FDA (registration 3001224205) in Koto-ku Tokyo, Japan. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 29, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3001224205
- Address
- 1-4-4 Furuishiba, Koto-ku Tokyo, Japan, 135-0045
- Owner or operator
- YA-MAN LTD. (10039976)
- Roles
- Exporter to the US, Specification developer
- First device listed
- February 26, 2012
- Registered through
- 2026
- Brand names listed
- L-SER KO, Medi Lift Essential, Medi Lift Essential Eye Mask, Medi Lift Mask, Medi Lift Pro, YA-MAN LTD.
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Specification developer | accessdata.fda.gov |
| Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy | NHN | 2 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Exporter to the US, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 29, 2025 | K250618 | Medi Lift Essential Eye Mask | NFO | Substantially Equivalent | Ya-Man, Ltd. | accessdata.fda.gov |
| January 16, 2025 | K244048 | Medi Lift Mask | NFO | Substantially Equivalent | Ya-Man, Ltd. | accessdata.fda.gov |
| June 28, 2023 | K220198 | Medi Lift PLUS | NFO | Substantially Equivalent | Ya-Man, Ltd. | accessdata.fda.gov |
| February 10, 2012 | K112016 | L-SER KO LAMP | ILY | Substantially Equivalent | Ya-Man, Ltd. | accessdata.fda.gov |
| April 15, 2010 | K100116 | LASERTOUCHONE (OTC) | NUH | Substantially Equivalent | Laser Health Technologies, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
- All makers of Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
Updated October 29, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.