Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007589160

FEI Number

3007589160

Entity Name

Midwest Medical Mfg

City/State/Country

Oakland, AR, US

Establishment Address

9614 Oakland Rd, Oakland, AR 72661, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MIDWEST MEDICAL MFG (Owner Number: 10029313)

Owner / Operator Contact Address

806 west road, Mountain Home, AR 72653, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Karalyst Asico asico Katalyst Asico

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HNF	Scissors, Ophthalmic	Ophthalmic	Class 1	886.4350	2009-05-03
HMR	Marker, Ocular	Ophthalmic	Class 1	886.4570	2013-07-02
HNQ	Hook, Ophthalmic	Ophthalmic	Class 1	886.4350	2009-05-03

Official Correspondent

Kevin Hurst

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MIDWEST MEDICAL MFG

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007589160. Last updated year: 2026. Please use registration number 3007589160 when referencing this establishment in official correspondence.