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Arias International Company

US

Last updated May 27, 2026

What Arias International Company makes

Arias International Company manufactures orthodontic tools, including reusable manual dental scalers and height-adjustable washbasin brackets for dental settings. Their product line also covers orthodontic pliers and orthodontic tubes, designed for dental and orthodontic procedures.

All devices are classified as Class I under regulatory frameworks, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. The company 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 Arias International Company manufacture?

Arias International Company specializes in dental and orthodontic tools. Their product line includes reusable manual dental scalers, height-adjustable washbasin brackets, orthodontic pliers, and orthodontic tubes. These devices are primarily designed for use in dental and orthodontic procedures, supporting clinical workflows in those settings.

Where is Arias International Company based?

Arias International Company is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

Which regulatory registries list devices manufactured by Arias International Company?

Devices from Arias International Company are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices that have been assigned a UDI, ensuring traceability and compliance with regulatory requirements.

How are devices manufactured by Arias International Company classified under regulatory frameworks?

All devices produced by Arias International Company fall under Class I classification. This classification is typically assigned to low-risk devices that pose minimal potential harm to patients, such as many dental and orthodontic tools. Class I devices often require less stringent regulatory oversight compared to higher-risk categories.

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

Information

Country
US
Address
—
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
874612729

Catalogue (6)

DeviceModel / ReferenceRegistriesClassStatus
Aico 7501064
FDA UDI
Class IActive
Aico 76000175
FDA UDI
Class IActive
Aico 7604901S
FDA UDI
Class IActive
Aico 7604790S
FDA UDI
Class IActive
Aico 9582530
FDA UDI
Class IActive
Aico 7601027
FDA UDI
Class IActive

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