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AVERY BIOMEDICAL DEVICES, INC.

US Last updated 22 Oct 2026

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Devices
9
Registries
GUDIDFDA PMAFDA
FDA recalls
0

Catalogue9

What AVERY BIOMEDICAL DEVICES, INC. makes

Avery Biomedical Devices, Inc. manufactures extramuscular diaphragm/phrenic nerve electrical stimulation systems, including the Avery Breathing Pacemaker System and spinal epidural electrodes for P.E.N.S. such as model E-355. These devices are designed to stimulate the phrenic nerve or diaphragm to assist with breathing function.

The company's devices are classified as Class III medical devices and are listed in the FDA PMA and FDA UDI registries. Avery Biomedical Devices, Inc. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Avery Biomedical Devices, Inc. manufacture?

Avery Biomedical Devices, Inc. manufactures extramuscular diaphragm/phrenic nerve electrical stimulation systems, including the Avery Breathing Pacemaker System and spinal epidural electrodes for P.E.N.S. such as model E-355, which are designed to stimulate the phrenic nerve or diaphragm to assist with breathing function.

Where is Avery Biomedical Devices, Inc. based?

Avery Biomedical Devices, Inc. is based in the United States, as indicated by the country field in the device data.

Which registries list the devices made by Avery Biomedical Devices, Inc.?

The devices made by Avery Biomedical Devices, Inc. are listed in the FDA PMA and FDA UDI registries, as specified in the LISTED IN field of the device data.

How are the devices from Avery Biomedical Devices, Inc. classified?

The devices from Avery Biomedical Devices, Inc. are classified as Class III medical devices, as stated in the DEVICE CLASSES field of the provided data.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
61 MALL DR, COMMACK, NY, 11725
FDA FEI number
2427696