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EyeTech Digital Systems

United States US-MF-000035001 Last updated 23 Oct 2026

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Devices
3
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue3

  • EyeOn Air Ref EyeOn-12WC

    Class I EUDAMED Active
  • EyeOn Elite Ref EyeOn-14WE

    Class I EUDAMED Active
  • EyeOn Go Ref EyeOn-10NE

    Class I EUDAMED Active

Authorised representatives

About

Empower communication with EyeTech's eye gaze technology, enabling independence for individuals facing speech and motor challenges.

From the manufacturer's own website. Source

What EyeTech Digital Systems makes

EyeTech Digital Systems manufactures eye gaze technology devices, including the EyeOn Go, EyeOn Air, and EyeOn Elite, which are designed to help individuals with speech and motor challenges communicate independently.

The company's devices are Class I and listed in the EUDAMED registry. EyeTech Digital Systems is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does EyeTech Digital Systems manufacture?

EyeTech Digital Systems manufactures eye gaze technology devices, including the EyeOn Go, EyeOn Air, and EyeOn Elite, which are designed to help individuals with speech and motor challenges communicate independently.

Where is EyeTech Digital Systems based?

EyeTech Digital Systems is based in the United States, as indicated by the country information provided in the device data.

Which registries list EyeTech Digital Systems' devices?

EyeTech Digital Systems' devices are listed in the EUDAMED registry, as specified in the device data. No other registries are mentioned for this company.

How are EyeTech Digital Systems' devices classified?

EyeTech Digital Systems' devices are classified as Class I, which is the lowest risk category for medical devices, as indicated in the device data.

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

Information

Country
United States
Address
2141 E Broadway Rd , Tempe, United States
Phone
+18885393832
PRRC contact
Juan Zoppetti
EUDAMED SRN
US-MF-000035001
FDA FEI number
3008994998