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Cryogenic Instruments & Equipment, Ltd.

United KingdomFDA 510(k) applicant, unverified

Devices
1

What Cryogenic Instruments & Equipment, Ltd. makes

Cryogenic Instruments & Equipment, Ltd. manufactures cryogenic probes, including The Fern Cryoprobe, designed for controlled freezing applications in medical procedures.

The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The products are listed in the U.S. regulatory system.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • The Fern Cryoprobe Ref K892237

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Cryogenic Instruments & Equipment, Ltd. have in the registry?

The registry currently lists 1 device for Cryogenic Instruments & Equipment, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cryogenic Instruments & Equipment, Ltd.'s devices?

Among its 1 most recently registered device, Cryogenic Instruments & Equipment, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Cryogenic Instruments & Equipment, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Cryogenic Instruments & Equipment, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cryogenic Instruments & Equipment, Ltd. in the registry?

The most recently registered devices listed for Cryogenic Instruments & Equipment, Ltd. include THE FERN CRYOPROBE.

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