EUCLID VISION CORPORATION

FDA Device Registration & Listing · Sterling, VA, US · Registration 3014175039

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
3014175039
FEI Number
3014175039
Entity Name
EUCLID VISION CORPORATION
City/State/Country
Sterling, VA, US
Establishment Address
45472 Holiday Drive, Suite 7, Sterling, VA 20166, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Euclid Vision Corporation (Owner Number: 10056673)
Owner / Operator Contact Address
45472 Holiday Drive, Sterling, VA 20166, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Boston XO Boston XO2 M700 USB Automated Perimeter Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear Euclid Orthokeratology (tisilfocon A) Contact Lens for Overnight Wear medmont meridia Advanced Topographer Classic medmont meridia Advanced Topographer Professional Medmont Meridia Advance Topographer Vantage

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQD Lens, Contact (Other Material) - Daily Ophthalmic Class 2 886.5916 2019-02-28
HPT Perimeter, Automatic, Ac-Powered Ophthalmic Class 1 886.1605 2024-08-02
MWL Lens, Contact (Rigid Gas Permeable), Extended Wear Ophthalmic Class 3 886.5916 2018-01-03
NUU Lens, Contact, Orthokeratology, Overnight Ophthalmic Class 3 886.5916 2018-01-03
MMQ Topographer, Corneal, Ac-Powered Ophthalmic Class 1 886.1350 2024-08-02

Official Correspondent

Sandra Freitez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Euclid Vision Corporation
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
K963512 Benz Research and Development Corp. BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY WEAR CONTACT LENS (CLEAR AND TINTED, LATHE-CUT FROM LENS BL 1997-07-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014175039. Last updated year: 2026. Please use registration number 3014175039 when referencing this establishment in official correspondence.
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