MIDWEST EYE LABORATORIES, INC.

FDA Device Registration & Listing · Eau Claire, WI, US · Registration 2183955

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
2183955
FEI Number
1000115724
Entity Name
MIDWEST EYE LABORATORIES, INC.
City/State/Country
Eau Claire, WI, US
Establishment Address
4606 COMMERCE VALLEY RD, SUITE 201, Eau Claire, WI 54701, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MIDWEST EYE LABORATORIES, INC. (Owner Number: 9001850)
Owner / Operator Contact Address
4606 Commerce Valley Rd, Suite 201, Eau Claire, WI 54701, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Ocular Conformer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQN Conformer, Ophthalmic Ophthalmic Class 2 886.3130 2009-02-18

Official Correspondent

MICHAEL BARRETT

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MIDWEST EYE LABORATORIES, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Other Registrations for Same Entity

Registration Number Establishment Name Location
2183958 MIDWEST EYE LABORATORIES, INC. ROCHESTER, MN, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183955. Last updated year: 2026. Please use registration number 2183955 when referencing this establishment in official correspondence.
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