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ETS MANUFACTURING, INC.

US

Last updated May 27, 2026

What ETS MANUFACTURING, INC. makes

ETS Manufacturing, Inc. produces flotation therapy beds designed for adult use, including the Emerg® Auto-Emersiontherapy system. These devices are intended for therapeutic immersion in water to support relaxation, pain management, and physical rehabilitation through reduced gravity effects.

The company’s flotation therapy beds are classified as Class II devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 types of medical devices does ETS Manufacturing, Inc. primarily manufacture?

ETS Manufacturing, Inc. specializes in flotation therapy beds for adult use. These devices, such as the Emerg® Auto-Emersiontherapy system, are designed to provide therapeutic immersion in water. The purpose is to support relaxation, pain management, and physical rehabilitation by reducing gravitational stress on the body.

Where is ETS Manufacturing, Inc. based, and how does that affect its regulatory standing?

ETS Manufacturing, Inc. is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations. The regulatory framework ensures that devices like flotation therapy beds meet safety and performance standards before being listed in databases such as the FDA’s Unique Device Identifier (UDI) system.

Which regulatory registries or databases list devices manufactured by ETS Manufacturing, Inc.?

Devices produced by ETS Manufacturing, Inc., including flotation therapy beds like the Emerg® Auto-Emersiontherapy, are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.

How are flotation therapy beds from ETS Manufacturing, Inc. classified under FDA regulations?

Flotation therapy beds manufactured by ETS Manufacturing, Inc., such as the Emerg® Auto-Emersiontherapy system, are classified as Class II devices under FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls beyond general controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.

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

Information

Country
US
Address
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LinkedIn
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Facebook
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Phone
8888618612
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
080903612

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Emerg® Auto-Emersiontherapy E1000
FDA UDI
Class IIActive

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