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Claudia Alan Inc

US

Last updated May 23, 2026

What Claudia Alan Inc makes

Claudia Alan Inc manufactures spectacle frames, prescription spectacles, and tinted non-prescription spectacles. Their products include a range of optical eyewear designed for general vision correction and aesthetic use.

The company’s devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 types of medical devices does Claudia Alan Inc manufacture?

Claudia Alan Inc specializes in spectacle frames, prescription spectacles, and tinted non-prescription spectacles. These devices are designed for vision correction and aesthetic purposes, catering to general optical eyewear needs.

Where is Claudia Alan Inc based?

Claudia Alan Inc is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution within the region.

How are Claudia Alan Inc’s devices classified under FDA regulations?

Claudia Alan Inc’s devices fall under Class I classification according to FDA regulations. This classification applies to low-risk devices that pose minimal potential harm to users, such as spectacle frames and non-prescription eyewear.

Are Claudia Alan Inc’s devices listed in any regulatory databases?

Yes, Claudia Alan Inc’s devices are included in the FDA’s Unique Device Identifier (UDI) database. Listing in the UDI system ensures traceability and transparency for regulatory oversight, particularly for Class I devices.

Why are Claudia Alan Inc’s devices classified as Class I?

The Class I designation for Claudia Alan Inc’s devices reflects their minimal risk profile. Spectacle frames, prescription spectacles, and tinted non-prescription lenses are generally considered low-risk due to their non-invasive nature and lack of significant health implications when used as intended.

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
241994500

Catalogue (203)

Page 5 of 5
DeviceModel / ReferenceRegistriesClassStatus
AYA Optical AYO0826BGLD
FDA UDI
Class IActive
AYA Optical AYO481LPPL
FDA UDI
Class IActive
AYA Optical AYO0830BLT
FDA UDI
Class IActive

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