Data / Medical devices / Clamp, Vascular / Japan
FDA-registered makers of Clamp, Vascular in Japan: 5 establishments
5 establishments in Japan are registered with the FDA to make Clamp, Vascular (product code DXC). 4 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
- Clamp, Vascular
- Product code
- DXC
- Country
- Japan
Makers of Clamp, Vascular in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bear Medic Corporation | Daigomachi, Kuji-gun Ibaraki, Japan | Manufacturer | 2 | August 18, 2016 | 0 | 0 | 0 | api.fda.gov |
| Ashitaka Factory Of Terumo Corp. | FUJINOMIYA Shizuoka, Japan | Specification developer | 1 | March 28, 2007 | 0 | 0 | 0 | api.fda.gov |
| Keisei Medical Industrial Co., Ltd. | BUNKYO-KU Tokyo, Japan | Manufacturer | 1 | March 26, 1999 | 0 | 0 | 0 | api.fda.gov |
| Kono Seisakusho | Ichikawa Chiba, Japan | Complaint file establishment, Manufacturer | 1 | October 23, 2023 | 0 | 0 | 0 | api.fda.gov |
| Diadem Corporation | Ibaraki, 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.