Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043520139

FEI Number

3043520139

Entity Name

Lightfield Medical Europe, S.L.U.

City/State/Country

Viladecans Barcelona, ES

Establishment Address

Carrer de Marie Curie, 54, Planta 4a (Poligon Ca n' Alemany), Viladecans Barcelona 08840, ES

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Lightfield Medical, Inc. (Owner Number: 10094221)

Owner / Operator Contact Address

3400 W Bde Maka Ska Pkwy, Minneapolis, MN 55416, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PUE	Biomicroscope, Slit-Lamp, Ac-Powered, Exempt	Ophthalmic	Class 2	886.1850	2025-11-19

Official Correspondent

No official correspondent registered.

US Agent Details

John Berestka Business: Lightfield Medical, Inc. Email: chip@lightfieldmedical.com Phone: (763) 4388697

Related Public Records

Same Entity

Lightfield Medical, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3042023395	LIGHTFIELD MEDICAL, INC.	Minneapolis, MN, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043520139. Last updated year: 2026. Please use registration number 3043520139 when referencing this establishment in official correspondence.