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Euclid Vision Corporation: FDA-registered device maker in Sterling, VA, United States, 1 510(k) clearance and 1 PMA approval

Name: Euclid Vision Corporation FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Euclid Vision Corporation is registered with the FDA (registration 3014175039) in Sterling, VA, United States. It lists 5 device types. The FDA files 1 510(k) clearance and 1 PMA approval under its listings, the newest dated September 29, 2004. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3014175039
Address: 45472 Holiday Drive Suite 7, Sterling, VA, United States, 20166
Owner or operator: Euclid Vision Corporation (10056673)
Roles: Complaint file establishment, Manufacturer
First device listed: January 3, 2018
Registered through: 2026
Brand names listed: Boston XO, Boston XO2, Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear, Euclid Orthokeratology (tisilfocon A) Contact Lens for Overnight Wear, M700 USB Automated Perimeter, Medmont Meridia Advance Topographer Vantage, medmont meridia Advanced Topographer Classic, medmont meridia Advanced Topographer Professional

Devices it lists

Device	Product code	Class	Role	Source
Lens, Contact (Other Material) - Daily	HQD	2	Manufacturer	accessdata.fda.gov
Lens, Contact (Rigid Gas Permeable), Extended Wear	MWL	3	Manufacturer	accessdata.fda.gov
Lens, Contact, Orthokeratology, Overnight	NUU	3	Manufacturer	accessdata.fda.gov
Perimeter, Automatic, Ac-Powered	HPT	1	Complaint file establishment	accessdata.fda.gov
Topographer, Corneal, Ac-Powered	MMQ	1	Complaint file establishment	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
April 3, 2002	K013762	RIGID GAS PERMEABLE CONTACT LENS	HQD	Substantially Equivalent	Bausch & Lomb, Incorporated	accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Approved	PMA number	Device	Product code	Supplements	Latest decision	Source
September 29, 2004	P040029	Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear and Euclid Orthokeratology (tisilfocon A) Contact	NUU	22	April 2, 2026	accessdata.fda.gov

Compare with other makers

Updated April 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.