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Mid-Canada Medical

CanadaFDA applicant, unverified

Devices
5

What Mid-Canada Medical makes

Mid-Canada Medical produces patient mobility and support devices, including the Parker Bathing System for assisted bathing, the Multi-Care Chair for seated mobility and positioning, and modifications to the Medi-Stim for therapeutic or assistive use.

The company’s portfolio includes Class I and Class II devices, with some products authorised via the FDA’s 510(k) pathway. These devices are listed under U.S. regulatory requirements, and the manufacturer operates from the United States.

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

Catalogue5

Newest first, rows 1-5 of 5

  • Parker Bathing System Ref K883308

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Mid-Canada Medical Ref K922839

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Medi-Stim, Modification Ref K933237

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Medi-Stim Ref K921491

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Multi-Care Chair Ref K883309

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

Frequently asked questions

How many devices does Mid-Canada Medical have in the registry?

The registry currently lists 5 devices for Mid-Canada Medical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mid-Canada Medical's devices?

Among its 5 most recently registered devices, Mid-Canada Medical has devices listed in FDA 510(k) (5 devices).

What risk classes do Mid-Canada Medical's devices fall under?

Among its 5 most recently registered devices, the classes recorded for Mid-Canada Medical's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Mid-Canada Medical in the registry?

The most recently registered devices listed for Mid-Canada Medical include PARKER BATHING SYSTEM, MID-CANADA MEDICAL, MEDI-STIM, MODIFICATION and MEDI-STIM.

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