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Spectrum Medical, LLP

United KingdomFDA applicant, unverified

Devices
2

What Spectrum Medical, LLP makes

Spectrum Medical, LLC manufactures patient monitoring devices, including the M4 Monitor and Spectrum M2 Monitor, which are designed for real-time vital sign tracking in clinical settings.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • M4 Monitor Ref K110957

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Spectrum M2 Monitor Ref K062468

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

Frequently asked questions

How many devices does Spectrum Medical, Llp have in the registry?

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

Which registries list Spectrum Medical, Llp's devices?

Among its 2 most recently registered devices, Spectrum Medical, Llp has devices listed in FDA 510(k) (2 devices).

What risk classes do Spectrum Medical, Llp's devices fall under?

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

What are the newest devices from Spectrum Medical, Llp in the registry?

The most recently registered devices listed for Spectrum Medical, Llp include M4 MONITOR and SPECTRUM M2 MONITOR.

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