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Anschel Technology, Inc.

US

Last updated May 30, 2026

What Anschel Technology, Inc. makes

Anschel Technology, Inc. manufactures visual stimulator devices, including portable units like the SightSaverMini and goggles such as the ADHERENT VISUAL STIMULATOR GOGGLES, designed to support visual function or rehabilitation.

These products fall under FDA Class II regulation and are listed under the 510(k) and UDI programs. The company 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 Anschel Technology, Inc. manufacture?

Anschel Technology, Inc. specializes in visual stimulator devices. These products are designed to assist with visual function or rehabilitation, including portable units like the SightSaverMini and goggles such as the ADHERENT VISUAL STIMULATOR GOGGLES. The focus is on supporting vision-related needs through innovative technology.

Where is Anschel Technology, Inc. based?

Anschel Technology, Inc. is headquartered in the United States. The company’s location ensures it operates within the regulatory framework of the FDA, which governs its device classifications and compliance requirements.

Which regulatory registries or programs list Anschel Technology, Inc.’s devices?

Anschel Technology, Inc.’s devices are listed under the FDA’s 510(k) premarket notification program and the Unique Device Identifier (UDI) system. These registries ensure traceability and compliance with U.S. medical device regulations, particularly for Class II devices.

How are Anschel Technology, Inc.’s devices classified by regulatory authorities?

Anschel Technology, Inc.’s visual stimulator devices are classified as FDA Class II. This classification is determined based on the risk associated with the device’s intended use and design, requiring compliance with specific controls to ensure safety and effectiveness.

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
966842036

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
SightSaverMini ATMV001
FDA UDI
Class IIActive
Adherent Visual Stimulator Goggles K113785
FDA 510(k)
Class IIActive

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