Kowa Co. Ltd. Chofu
JapanFDA 510(k) applicant, unverified FDA FEI 3011223751
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Kowa Co. Ltd. Chofu makes
Kowa Co. Ltd. manufactures the VK-2s, a surgical microscope designed for precision ophthalmic procedures, including cataract and retinal surgeries.
The VK-2s is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
KOWA VK-2s Ref K190056
510(k) 510(k)
Company details
- FDA FEI number
- 3011223751
- Address
- 3-1, Chofugaoka 3-chome, Chofu Tokyo
Frequently asked questions
How many devices does Kowa Co. Ltd. Chofu have in the registry?
The registry currently lists 1 device for Kowa Co. Ltd. Chofu. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kowa Co. Ltd. Chofu's devices?
Among its 1 most recently registered device, Kowa Co. Ltd. Chofu has devices listed in FDA 510(k) (1 device).
What risk classes do Kowa Co. Ltd. Chofu's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kowa Co. Ltd. Chofu's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kowa Co. Ltd. Chofu in the registry?
The most recently registered devices listed for Kowa Co. Ltd. Chofu include KOWA VK-2s.