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Flocare Medical

Country not established

Devices
4

What Flocare Medical makes

Flocare Medical manufactures single-use, disposable medical devices designed for respiratory care, including ventilator circuits, breathing tubes, and sampling ports for patient monitoring. Their product line includes models for both humidified and non-humidified ventilation systems, as well as specialized ports for dry gas sampling in critical care settings.

The company’s devices are classified under Class I in the U.S. regulatory framework and are listed via 510(k) clearance with the FDA. Their portfolio is intended for use in clinical environments requiring sterile, single-patient-use respiratory support components.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Flocare F Ref K903404

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Flocare Lf-A Ref K912699

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Flocare Dry Cas Sampling Port Models Ref K912700

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Flocare N Ref K902501

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

Frequently asked questions

How many devices does Flocare Medical have in the registry?

The registry currently lists 4 devices for Flocare Medical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Flocare Medical's devices?

Among its 4 most recently registered devices, Flocare Medical has devices listed in FDA 510(k) (4 devices).

What risk classes do Flocare Medical's devices fall under?

Among its 4 most recently registered devices, the classes recorded for Flocare Medical's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Flocare Medical in the registry?

The most recently registered devices listed for Flocare Medical include FLOCARE F, FLOCARE LF-A, FLOCARE DRY CAS SAMPLING PORT MODELS and FLOCARE N.

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