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Piper Medical Products

Country not established

Devices
3

What Piper Medical Products makes

Piper Medical Products manufactures portable nebulizers, including the EZFLOW MAX (Model 1007) and EZFLOW Continuous Nebulizer (Model 1005), designed for delivering aerosolized medication. Their product line also includes the AEROTEE (Model #1001), a handheld nebulizer system for respiratory therapy. These devices are intended for use in home and clinical settings to administer inhaled treatments.

All listed devices fall under FDA Class II regulation and are authorised via 510(k) clearance. The company operates from the United States, with its products registered in the FDA’s 510(k) database.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Ezflow Max, Model 1007 Ref K993558

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ezflow Continuous Nebulizer, Model 1005 Ref K990384

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Aerotee, Model # 1001 Ref K982408

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

Frequently asked questions

How many devices does Piper Medical Products have in the registry?

The registry currently lists 3 devices for Piper Medical Products. Devices recorded under merged duplicate company entries are counted once.

Which registries list Piper Medical Products's devices?

Among its 3 most recently registered devices, Piper Medical Products has devices listed in FDA 510(k) (3 devices).

What risk classes do Piper Medical Products's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Piper Medical Products's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Piper Medical Products in the registry?

The most recently registered devices listed for Piper Medical Products include EZFLOW MAX, MODEL 1007, EZFLOW CONTINUOUS NEBULIZER, MODEL 1005 and AEROTEE, MODEL # 1001.

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