MIDWEST EYE LABORATORIES, INC.

FDA Device Registration & Listing · ROCHESTER, MN, US · Registration 2183958

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
2183958
FEI Number
1000116180
Entity Name
MIDWEST EYE LABORATORIES, INC.
City/State/Country
ROCHESTER, MN, US
Establishment Address
20 2ND AVE., S.W., SUITE 223, ROCHESTER, MN 55901, 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

SHELL SCLERAL SCLERAL SHELL Ocular Conformer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQT Shell, Scleral Ophthalmic Class 2 886.3800 2001-12-13
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
2183955 MIDWEST EYE LABORATORIES, INC. Eau Claire, WI, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183958. Last updated year: 2026. Please use registration number 2183958 when referencing this establishment in official correspondence.
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