Ashitaka Factory of Terumo Corporation

JP Last updated 22 Oct 2026

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Devices: 6
Registries: FDA 510(k)FDA
FDA recalls: 0

Catalogue6

FineCross M3 Ref K203521

Class II FDA 510(k) Active
Radifocus Glidewire Ref K152740

Class II FDA 510(k) Active
Radifocus Optitorque Angiographic Catheter Ref K150232

Class II FDA 510(k) Active
Progreat Ref K170223

Class II FDA 510(k) Active
Capiox FX15 And FX25 Hollow Fiber Oxygenator/Reservoir Ref K130520

Class II FDA 510(k) Active
R2P SlenGuide Ref K161546

Class II FDA 510(k) Active

FDA establishments1

Registered with the FDA under this company group, matched by name.

Ashitaka Factory Of Terumo Corp. FUJINOMIYA Shizuoka · JP FEI 3002808327

Information

Country: JP