SIGHT ENHANCEMENT TECHNOLOGIES

FDA Device Registration & Listing · Midland Ontario, CA · Registration 3003263095

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
3003263095
FEI Number
3003263095
Entity Name
SIGHT ENHANCEMENT TECHNOLOGIES
City/State/Country
Midland Ontario, CA
Establishment Address
263 Barnett Ave., Midland Ontario L4R 1N3, CA
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Sight Enhancement Technologies (Owner Number: 10025609)
Owner / Operator Contact Address
263 Barnett Ave., Midland, CA-ON L4R 1N3, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SET Prism Reader

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2008-04-23

Official Correspondent

Jaime Lovegrove

US Agent Details

Gina Carey Business: Eschenbach Optik of America, Inc Email: gcarey@eschenbach.com Phone: (203) 7021605

Related Public Records

Same Entity

Sight Enhancement Technologies
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003263095. Last updated year: 2026. Please use registration number 3003263095 when referencing this establishment in official correspondence.
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