Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1821850

FEI Number

1821850

Entity Name

MICHIGAN INSTRUMENTS

City/State/Country

Grand Rapids, MI, US

Establishment Address

4717 Talon Ct SE, Grand Rapids, MI 49512, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

Michigan Instruments (Owner Number: 10058057)

Owner / Operator Contact Address

4717 Talon Court SE, Grand Rapids, MI 49512, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Thumper Model 1007CC Thumper Model 1008 Thumper Model 1007SC Thumper Model 1007SCV Thumper Model 1007CCV Thumper Model 1008G

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRM	Compressor, Cardiac, External	Cardiovascular	Class 2	870.5200	2023-06-29

Official Correspondent

Chris Blanker

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Michigan Instruments

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 1821850. Last updated year: 2026. Please use registration number 1821850 when referencing this establishment in official correspondence.