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Penox Technologies, Inc.

United StatesFDA applicant, unverified

Devices
10

What Penox Technologies, Inc. makes

Penox Technologies, Inc. manufactures medical mobility and oxygen delivery devices, including manual and modified lift chairs, wheelchair accessories like T-handle and U-handle adapters, and hospital beds. Their portfolio also includes oxygen therapy equipment such as high-flow manifolds, dual-flow minifolds, dual-feed manifolds, and portable liquid oxygen units. Additional products include fill hose safety adapters and a performer wheelchair designed for patient mobility.

The company’s devices are regulated under FDA Class I and Class II classifications, with most products listed via the 510(k) pathway. These products are registered in the FDA’s 510(k) database, and the company is based in the United States.

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

Catalogue10

Newest first, rows 1-10 of 10

  • Penox Lift Chair Ref K851218

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

  • Penox High Flow Manifold Ref K853775

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

  • T-Handle Adapter, U-Handle & L Handler Adapter Ref K851215

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

  • Fill Hose Safety Adapter Ref K851219

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

  • Portable Liquid Oxygen Unit (Modification) Ref K863978

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

  • Modified Penox Lift Chair Ref K862654

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

  • Penox Dual Flow Minifold Ref K851217

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

  • Penox Dual Feed Manifold Ref K851216

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

  • Penox Performer Wheelchair Ref K852109

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

  • Penox Hospital Bed Ref K864667

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

Frequently asked questions

How many devices does Penox Technologies, Inc. have in the registry?

The registry currently lists 10 devices for Penox Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Penox Technologies, Inc.'s devices?

Among its 10 most recently registered devices, Penox Technologies, Inc. has devices listed in FDA 510(k) (10 devices).

What risk classes do Penox Technologies, Inc.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Penox Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Penox Technologies, Inc. in the registry?

The most recently registered devices listed for Penox Technologies, Inc. include PENOX LIFT CHAIR, PENOX HIGH FLOW MANIFOLD, T-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTER and FILL HOSE SAFETY ADAPTER.

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