Ya-Man, Ltd.
Country not established FDA
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Ya-Man, Ltd. makes
Ya-Man, Ltd. manufactures transcutaneous neuromuscular electrical stimulation (TENS) systems for physical therapy, including models like the Medi Lift and Medi Lift PLUS. The company also produces laser therapy devices, such as the LASER 20 and YA-MAN LASER 21, as well as LED-based lamps like the L-SER KO LAMP and eye masks for therapeutic use.
These devices are classified as Class II under US regulations and are authorised via the FDA’s 510(k) pathway and the Unique Device Identifier (UDI) system. Ya-Man, Ltd. is based in the United States.
Catalogue
Search and filter all 11 devicesCompany details
- DUNS number
- 690652508
FDA establishments
- Ya-Man Ltd. Koto-ku Tokyo · JP FEI 3001224205
Frequently asked questions
How many devices does Ya-Man, Ltd. have in the registry?
The registry currently lists 11 devices for Ya-Man, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ya-Man, Ltd.'s devices?
Among its 11 most recently registered devices, Ya-Man, Ltd. has devices listed in FDA 510(k) (6 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Ya-Man, Ltd.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Ya-Man, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ya-Man, Ltd. in the registry?
The most recently registered devices listed for Ya-Man, Ltd. include Medi Lift EPM-18GW, Medi Lift EPE-10, Medi Lift EPM-18-G and Medi Lift EPM-18-GC.
Which FDA establishments are linked to Ya-Man, Ltd.?
1 FDA establishment is linked to Ya-Man, Ltd. in the registry; they are listed on the company page.