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ASSOCIATED INDUSTRIES CHINA, INC.

US

Last updated May 24, 2026

What ASSOCIATED INDUSTRIES CHINA, INC. makes

The company manufactures dental power tool systems, including pneumatic and line-powered handpieces designed for precision dental procedures. It also produces dental delivery systems for fluid or air distribution in clinical settings and steam sterilizers for instrument reprocessing. The AG Neovo series is a recurring product line across these categories.

These devices are classified under FDA regulations as Class I and Class II, with all products listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States and adheres to applicable U.S. regulatory requirements for medical devices.

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 Associated Industries China, Inc. manufacture?

Associated Industries China, Inc. specializes in dental devices, including pneumatic and line-powered dental power tool systems like handpieces for precision procedures, dental delivery systems for fluid or air distribution in clinical settings, and steam sterilizers for instrument reprocessing. Their product line often features the AG Neovo series across these categories.

Where is Associated Industries China, Inc. based?

The company is headquartered in the United States. This location ensures compliance with U.S. regulatory requirements for the medical devices it manufactures, including those listed in the FDA’s Unique Device Identifier (UDI) database.

Which regulatory registries list devices manufactured by Associated Industries China, Inc.?

Devices from Associated Industries China, Inc. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry tracks and identifies medical devices authorized for use in the U.S., ensuring traceability and compliance with regulatory standards.

How are the devices produced by Associated Industries China, Inc. classified under FDA regulations?

The company’s devices fall under two FDA classification tiers: Class I and Class II. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. Classification depends on factors like intended use and potential harm.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
656068681

Catalogue (28)

DeviceModel / ReferenceRegistriesClassStatus
AG Neovo REVOLUTION R-6500N
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6100K
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6510N
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6800B2
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6110WH
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6110DPS
FDA UDI
Class IActive
AG Neovo REVOLUTION R-2000
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6500K
FDA UDI
Class IActive
AG Neovo REVOLUTION R-4000
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6110S
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6110K
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6510DPS
FDA UDI
Class IActive
AG Neovo REVOLUTION R-1104
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6110N
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6500M4
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6100S
FDA UDI
Class IActive
AG Neovo AG neovo Dental Portable Dental Equipment PDE series PDE-181
FDA UDI
Class IActive
AG Neovo REVOLUTION R-2005
FDA UDI
Class IActive
AG Neovo Louie P-M10TR
FDA UDI
Class IIActive
AG Neovo REVOLUTION R-5500
FDA UDI
Class IActive
AG Neovo REVOLUTION R-5510
FDA UDI
Class IActive
AG Neovo REVOLUTION R-2010
FDA UDI
Class IActive
AG Neovo REVOLUTION R-1105
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6510K
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6100N
FDA UDI
Class IActive
AG Neovo REVOLUTION R-6510WH
FDA UDI
Class IActive
AG Neovo REVOLUTION R-4010
FDA UDI
Class IActive
AG Neovo REVOLUTION R-4005
FDA UDI
Class IActive

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