FDA applicant

Cryomedical Instruemts, Ltd.

Mansfield Woodhouse, Notts, GB1 decision2003–20030 recalls

FDA records 1 decision for Cryomedical Instruemts, Ltd. (Mansfield Woodhouse, Notts, GB) in 2003: 1 510(k) clearance. All are in product code GXH (Device, Surgical, Cryogenic). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Cryomedical Instruemts, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cryomedical Instruemts, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cryomedical Instruemts, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cryomedical Instruemts, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Cryomedical”

FDA records each applicant name separately; these may or may not be the same firm.

Cryomedical Sciences, Inc. 10 Cryomedical Instruments, Ltd. 1

Cryomedical Instruemts, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cryomedical”