MIDWEST PRODUCTS AND ENGINEERING

FDA Device Registration & Listing · Milwaukee, WI, US · Registration 3003500271

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
3003500271
FEI Number
3003500271
Entity Name
MIDWEST PRODUCTS AND ENGINEERING
City/State/Country
Milwaukee, WI, US
Establishment Address
10597 W Glenbrook Ct, Milwaukee, WI 53224, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Midwest Products and Engineering (Owner Number: 10043161)
Owner / Operator Contact Address
10597 Glenbrook Ct, Milwaukee, WI 53224, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Smart Scale - Rapid Weigh SS60 Sterrad Cart Paradigm SCMC3 Helix Cart mBos TKA System HealthChek Network Health Station INTELLIO VIDEO CART AVEO-TANK-MED AVEO-CART-PKG AVEO-TANK-LRG AVEO-TANK-SML SCMC1 REAL INTELLIGENCE™ CORI™ XT (CORI XT) RetCam Envision Assembly, Flex Ent 120V (9736179)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRW Scale, Patient General Hospital Class 1 880.2720 2020-06-16
INW Table, Mechanical Physical Medicine Class 1 890.3750 2013-01-28
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2023-06-23
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2019-02-27
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2016-09-07
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2025-08-25
FRW Scale, Patient General Hospital Class 1 880.2720 2021-03-09
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2021-03-09
NBH Accessories, Arthroscopic Orthopedic Class 1 888.1100 2023-12-26
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2023-09-11
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2019-02-27
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2026-01-20
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2021-04-27
PGW Ear, Nose, And Throat Stereotaxic Instrument Neurology Class 2 882.4560 2021-06-22

Official Correspondent

Jim Gartzke

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Midwest Products and Engineering
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K260601 Blue Belt Technologies, Inc. REAL INTELLIGENCE™ CORI™ 2026-03-26
K172344 Medax Srl Unipersonale Medax Biopsy Systems II (MEDONE, MEDCUT, MEDEM, MEDBONE, MEDLOCK) 2017-11-13
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0041-2024 Blue Belt Technologies, Inc 2
Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299
Z-0027-2024 Bard Peripheral Vascular Inc 2
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Z-0028-2013 Remington Medical Inc. 2
Automatic Cutting Needles, Soft Tissue Biopsy Needle, NAC-1820M, Sterile, Remington Medical, Inc., 5830 Meadowridge Court, Alpharetta, GA 30005. Prostate Biopsy Needles shall be single use only and are to be used by a Urologist in a healthcare setting to obtain needle biopsies of the prostate. The needles are compatible with the Bard Magnum biopsy instrument. The needles have an echogenic tip for accurate placement under ultrasound guidance and centimeter markings along the cannula to facilitate depth placement.
Z-0042-2014 Atossa Genetics, Inc. 2
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity System Kits, MASCT Patient Sample Kits & Clarity Patient Sample Kits Instrument, Biopsy. The MASCT System Kit, Patient Sample Kits, or the Nipple Aspirate Fluid Laboratory Kit has the following codes: PRODUCT CODE: AG-MASCT; AG-FC5; DTG-MASCT, DTG-FC5, and NRLBH-5. PART NUMBER: 9002513; 9002513MD; 9002528; 9002528MD; 9002587; 9002614; and 9002717MD. THE MASCT SYSTEM KIT CONSISTS OF: 1. MASCT Breast Pump; 2. Instructions for Use (IFU); 3. Heating Pad; 4. Timer; 5. Saccomono's Fixative; 6. Nu Prep Gel; 7. Welcome and Training Materials Coversheet; 8. MASCT System Order Form; 9. ForeCYTE Training Video DVD; 10. MASCT System Instructions with pictures - pink; THE PATIENT SAMPLE KIT CONSISTS OF: 1. Two (2) flower assemblies (e.g., filter, filter retainer, and filter holder); 2. Instructions for Use (IFU); 3. Two (2) specimen collection devices; 4. Two (2) breast bags for transporting the specimen collection container; 5. Barcode labels; 6. Saccomono's Fixative; 7. Nu Prep Gel; 8. MASCT System package insert; 9. ForeCYTE Test Requisition Form; 10. Patient Information Sheet; 11. Atossa Patient Information; 12. FED EX Clinical PAK; 13. MASCT System Order Form; 14. FED EX Pouch; 15. FED EX Airbill; Product Usage: The MASCT Device is intended for use in the collection of nipple aspirate fluid for cytological testing. The collected fluid can be used in the determination and/or differentiation of normal versus premalignant versus malignant cells.
Z-0044-2018 Bard Peripheral Vascular Inc 2
BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18 g x 16 cm; MC1820, 18 g x 20 cm; MC1825, 18 g x 25 cm. The core needle biopsy device is intended for use in obtaining biopsies from soft tissues.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003500271. Last updated year: 2026. Please use registration number 3003500271 when referencing this establishment in official correspondence.
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