MIDWEST EYE LABORATORIES SIOUX FALLS LLC

FDA Device Registration & Listing · SIOUX FALLS, SD, US · Registration 2183957

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
2183957
FEI Number
1000116181
Entity Name
MIDWEST EYE LABORATORIES SIOUX FALLS LLC
City/State/Country
SIOUX FALLS, SD, US
Establishment Address
4921 E. 26th St., Suite 2, SIOUX FALLS, SD 57110, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Precise Ocular Prosthetics LLC (Owner Number: 10036013)
Owner / Operator Contact Address
7582 Currell Blvd., Suite 109, Woodbury, MN 55125, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

OCULAR PROSTHESIS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQH Eye, Artificial, Non-Custom Ophthalmic Class 1 886.3200 2011-04-13

Official Correspondent

Timothy Barrett

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Precise Ocular Prosthetics LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2183831 MIDWEST EYE LABORATORIES WOODBURY LLC Saint Paul, MN, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183957. Last updated year: 2026. Please use registration number 2183957 when referencing this establishment in official correspondence.
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