LIGHTFIELD MEDICAL, INC.

FDA Device Registration & Listing · Minneapolis, MN, US · Registration 3042023395

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
3042023395
FEI Number
3042023395
Entity Name
LIGHTFIELD MEDICAL, INC.
City/State/Country
Minneapolis, MN, US
Establishment Address
3400 W Bde Maka Ska Pkwy, Minneapolis, MN 55416, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
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
N
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

No US Agent registered (Local establishment).

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
3043520139 Lightfield Medical Europe, S.L.U. Viladecans Barcelona, ES

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042023395. Last updated year: 2026. Please use registration number 3042023395 when referencing this establishment in official correspondence.
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