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Lms Medical Systems, Ltd.

CanadaFDA applicant, unverified

Devices
2
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

Catalogue2

Newest first, rows 1-2 of 2

  • Calm Ref K980719

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Calm Patterns, Version 01.00.00 Ref K040788

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

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

  • 2005

    • 11 Jan 2005 Z-0821-06 Unclassified (pre-2012) Terminated A deficiency in the software code can, in certain circumstances, cause data for the wrong patient to be displayed in the Tracing Review screen when a user is acknowledging an Alert Distribution: AL, IL, MD, NH, OH and Canada

Frequently asked questions

How many devices does Lms Medical Systems, Ltd. have in the registry?

The registry currently lists 2 devices for Lms Medical Systems, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lms Medical Systems, Ltd.'s devices?

Among its 2 most recently registered devices, Lms Medical Systems, Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do Lms Medical Systems, Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Lms Medical Systems, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Lms Medical Systems, Ltd.?

FDA recall records list 1 recall initiated by Lms Medical Systems, Ltd., the most recent initiated on 11 Jan 2005. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Lms Medical Systems, Ltd. in the registry?

The most recently registered devices listed for Lms Medical Systems, Ltd. include CALM and CALM PATTERNS, VERSION 01.00.00.

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