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Olympus Shirakawa Co., Ltd.

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Devices
1

What Olympus Shirakawa Co., Ltd. makes

Olympus Shirakawa Co., Ltd. manufactures the PSD-60 Endoplasma, a device designed for endoscopic plasma coagulation used in medical procedures.

The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Psd-60/Endoplasma Ref K042274

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Olympus Shirakawa Co., Ltd. have in the registry?

The registry currently lists 1 device for Olympus Shirakawa Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Olympus Shirakawa Co., Ltd.'s devices?

Among its 1 most recently registered device, Olympus Shirakawa Co., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Olympus Shirakawa Co., Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Olympus Shirakawa Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Olympus Shirakawa Co., Ltd. in the registry?

The most recently registered devices listed for Olympus Shirakawa Co., Ltd. include PSD-60/ENDOPLASMA.

Generated automatically from registry data and not verified by a human reviewer.