Data / Medical devices / Wire, Guide, Catheter / Japan
FDA-registered makers of Wire, Guide, Catheter in Japan: 11 establishments
11 establishments in Japan are registered with the FDA to make Wire, Guide, Catheter (product code DQX). 8 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
- Wire, Guide, Catheter
- Product code
- DQX
- Country
- Japan
Makers of Wire, Guide, Catheter 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 | 49 | April 2, 2025 | 0 | 0 | 0 | api.fda.gov |
| Ashitaka Factory Of Terumo Corp. | FUJINOMIYA Shizuoka, Japan | Contract manufacturer, Manufacturer | 14 | November 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| Filmecc Co., Ltd. | Seto-shi Aichi, Japan | Complaint file establishment, Manufacturer, Specification developer | 8 | September 3, 2026 | 0 | 0 | 0 | api.fda.gov |
| FMD. Co., Ltd. | Komaki Aichi, Japan | Manufacturer, Specification developer | 5 | June 13, 2024 | 0 | 0 | 0 | api.fda.gov |
| FMD Co., Ltd. Okinawa Factory | Uruma Okinawa, Japan | Contract manufacturer, Manufacturer | 2 | June 13, 2024 | 0 | 0 | 0 | api.fda.gov |
| Nipro Medical Industries Ltd. | TATEBAYASHI-SHI Gunma, Japan | Manufacturer | 1 | July 7, 2000 | 0 | 0 | 0 | api.fda.gov |
| Toray Industries, Inc. | CHUO-KU Tokyo, Japan | Complaint file establishment, Specification developer | 1 | December 17, 2004 | 0 | 0 | 0 | api.fda.gov |
| Toray Industries, Inc. Seta Plant | OTSU Shiga, Japan | Manufacturer | 1 | December 17, 2004 | 0 | 0 | 0 | api.fda.gov |
| Piolax Medical Devices, Inc. | Yokohama Kanagawa, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Terumo Yamaguchi Corporation | Yamaguchi-shi, Japan | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yokowo Co., Ltd | Tomioka Gunma, Japan | Contract manufacturer | 0 | 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.