Ashitaka Factory of Terumo Corporation
JapanFDA applicant, unverified FDA
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
Catalogue
FineCross M3 Ref K203521
Regimes: 510(k) Registry: 510(k)Radifocus Glidewire Ref K152740
Regimes: 510(k) Registry: 510(k)Radifocus Optitorque Angiographic Catheter Ref K150232
Regimes: 510(k) Registry: 510(k)Progreat Ref K170223
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
R2P SlenGuide Ref K161546
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Ashitaka Factory Of Terumo Corp. FUJINOMIYA Shizuoka · JP FEI 3002808327
Frequently asked questions
How many devices does Ashitaka Factory of Terumo Corporation have in the registry?
The registry currently lists 6 devices for Ashitaka Factory of Terumo Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ashitaka Factory of Terumo Corporation's devices?
Among its 6 most recently registered devices, Ashitaka Factory of Terumo Corporation has devices listed in FDA 510(k) (6 devices).
What risk classes do Ashitaka Factory of Terumo Corporation's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Ashitaka Factory of Terumo Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ashitaka Factory of Terumo Corporation in the registry?
The most recently registered devices listed for Ashitaka Factory of Terumo Corporation include FineCross M3, Radifocus Glidewire, Radifocus Optitorque Angiographic Catheter and Progreat.
Which FDA establishments are linked to Ashitaka Factory of Terumo Corporation?
1 FDA establishment is linked to Ashitaka Factory of Terumo Corporation in the registry; they are listed on the company page.