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NEXUS OPTICAL, INC.

US

Last updated May 23, 2026

What NEXUS OPTICAL, INC. makes

Nexus Optical, Inc. manufactures multi-purpose solutions designed for cleaning, disinfecting, and storing soft contact lenses. These solutions are formulated to maintain lens hygiene and ensure compatibility with daily, biweekly, and monthly wear schedules.

The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. Nexus Optical, Inc. is headquartered 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 Nexus Optical, Inc. manufacture?

Nexus Optical, Inc. specializes in multi-purpose soft contact lens solutions. These solutions are formulated to clean, disinfect, and store soft contact lenses, supporting various wear schedules like daily, biweekly, and monthly use. The focus is on maintaining lens hygiene and compatibility with different contact lens materials.

Where is Nexus Optical, Inc. based?

Nexus Optical, Inc. is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and operational base, particularly when assessing compliance with U.S. medical device regulations.

Which regulatory registries or databases list Nexus Optical, Inc.’s devices?

Nexus Optical, Inc.’s devices 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 Nexus Optical, Inc.’s devices classified under U.S. regulations?

Nexus Optical, Inc.’s multi-purpose soft contact lens solutions are classified as Class II medical devices under FDA regulations. This classification typically indicates moderate risk, requiring specific controls to ensure 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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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
107289657

Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Nexus Optical Aquanu 12 Fl Oz
FDA UDI
Class IIActive
Nexus Optical Cove 12 Fl Oz
FDA UDI
Class IIActive
Nexus Optical Aquanu 4 Fl Oz
FDA UDI
Class IIActive
Nexus Optical Cove 4 Fl Oz
FDA UDI
Class IIActive

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