Skip to content

Yozma Bmtech Co., Ltd.

South KoreaFDA applicant, unverified

Devices
1

What Yozma Bmtech Co., Ltd. makes

Yozma Bmtech Co., Ltd. manufactures the Frozen N, a medical device designed for cryopreservation applications in a clinical setting.

The Frozen N is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Frozen N Ref K193665

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

Frequently asked questions

How many devices does Yozma Bmtech Co., Ltd. have in the registry?

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

Which registries list Yozma Bmtech Co., Ltd.'s devices?

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

What risk classes do Yozma Bmtech Co., Ltd.'s devices fall under?

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

What are the newest devices from Yozma Bmtech Co., Ltd. in the registry?

The most recently registered devices listed for Yozma Bmtech Co., Ltd. include Frozen N.

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