Data / Medical devices / Japan / Sanyoseiko Co., Ltd.
Sanyoseiko Co., Ltd.: FDA-registered device maker in Otsuki-shi Yamanashi, Japan, 1 510(k) clearance
Sanyoseiko Co., Ltd. is registered with the FDA (registration 3011504786) in Otsuki-shi Yamanashi, Japan. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 8, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011504786
- Address
- 1150, Shimowada, Nanaho-machi, Otsuki-shi Yamanashi, Japan, 409-0622
- Owner or operator
- SANYOSEIKO CO., LTD. (10054424)
- Roles
- Manufacturer
- First device listed
- December 21, 2018
- Registered through
- 2026
- Brand names listed
- PS-2100
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Vibration Threshold Measurement | LLN | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| January 8, 2009 | K072882 | PAIN VISION, MODEL PS-2100 | LLN | Substantially Equivalent | Osachi Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 8, 2009. 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.