Data / Medical devices / Catheter, Percutaneous / Japan
FDA-registered makers of Catheter, Percutaneous in Japan: 5 establishments
5 establishments in Japan are registered with the FDA to make Catheter, Percutaneous (product code DQY). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Catheter, Percutaneous
- Product code
- DQY
- Country
- Japan
Makers of Catheter, Percutaneous in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Asahi Intecc Co., Ltd. | SETO Aichi, Japan | Manufacturer, Specification developer | 12 | June 25, 2024 | 0 | 0 | 0 | api.fda.gov |
| Ashitaka Factory Of Terumo Corp. | FUJINOMIYA Shizuoka, Japan | Contract manufacturer, Manufacturer | 4 | March 3, 2021 | 0 | 0 | 0 | api.fda.gov |
| FUJI SYSTEMS CORPORATION, Shin-Shirakawa Plant | Shirakawa Fukushima, Japan | Manufacturer | 1 | August 9, 2012 | 0 | 0 | 0 | api.fda.gov |
| FUJI SYSTEMS CORPORATION, Shirakawa Plant | Nishi Shirakawa Gun Fukushima, Japan | Manufacturer | 1 | August 9, 2012 | 0 | 0 | 0 | api.fda.gov |
| Kaneka Corporation Osaka Plant | Settsu-shi Osaka, Japan | Manufacturer | 1 | August 3, 2015 | 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.