REHAN ELECTRONICS

FDA Device Registration & Listing · Carnew Wexford, IE · Registration 3009840810

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009840810
FEI Number
3009840810
Entity Name
REHAN ELECTRONICS
City/State/Country
Carnew Wexford, IE
Establishment Address
Aughrim Road, Carnew Wexford Y14NY60, IE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Rehan Electronics (Owner Number: 10086622)
Owner / Operator Contact Address
Aughrim Road, Carnew, IE-WX Y14NY60, IE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Looky i-Reader 2 i-See Acuity Acuity i-See

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HPG Aid, Vision, Electronic, Battery-Powered Ophthalmic Class 1 886.5900 2022-11-25
HJG System, Reading, Television, Closed-Circuit Ophthalmic Class 1 886.5820 2022-12-06

Official Correspondent

Seamus Doyle

US Agent Details

Jeff Gardner Business: IRIE AT Email: sales@irie-at.com Phone: (541) 3603007

Related Public Records

Same Entity

Rehan Electronics
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K920069 Innoventions, Inc. MAGNI-CAM 1992-03-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009840810. Last updated year: 2026. Please use registration number 3009840810 when referencing this establishment in official correspondence.
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