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Data / Medical devices / United States / Mid Central Medical

Mid Central Medical: FDA-registered device maker in Saint Vincent, MN, United States, 1 510(k) clearance

Mid Central Medical is registered with the FDA (registration 3007886583) in Saint Vincent, MN, United States. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 20, 2010. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3007886583
Address
1401 Pacific Ave, Saint Vincent, MN, United States, 56755
Owner or operator
Mid Central Medical Corp (10050937)
Roles
Manufacturer, Specification developer
First device listed
January 19, 2016
Registered through
2026
Brand names listed
Mid Central Medical

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
September 20, 2010K101689EMM EQUIPMENT COVER-POLYTHYLENEKKXSubstantially EquivalentExact Medical Manufacturing, Inc.accessdata.fda.gov

Compare with other makers

Updated September 20, 2010. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.