Data / Medical devices / Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days / Japan
FDA-registered makers of Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days in Japan: 5 establishments
5 establishments in Japan are registered with the FDA to make Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days (product code FOZ). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- Product code
- FOZ
- Country
- Japan
Makers of Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Togo Medikit Co., Ltd. | HYUGA CITY Miyazaki, Japan | Complaint file establishment, Exporter to the US, Manufacturer | 3 | September 20, 2019 | 0 | 0 | 0 | api.fda.gov |
| Togo Medikit Co., Ltd. Medikit Hyuga Second Factory | Hyuga City Miyazaki, Japan | Manufacturer | 3 | September 20, 2019 | 0 | 0 | 0 | api.fda.gov |
| Kofu Factory Of Terumo Corp. | NAKAKOMA-GUN Yamanashi, Japan | Manufacturer | 2 | February 26, 2010 | 0 | 0 | 0 | api.fda.gov |
| Nipro Corporation Odate Factory | ODATE-SHI Akita, Japan | Manufacturer | 1 | March 28, 1996 | 0 | 0 | 0 | api.fda.gov |
| Nipro Medical Industries Ltd. | TATEBAYASHI-SHI Gunma, Japan | Manufacturer | 1 | December 5, 2013 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.