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Data / Medical devices / United States / OPS Center (for Mobia Medical Inc.)

OPS Center (for Mobia Medical Inc.): FDA-registered device maker in Minneapolis, MN, United States, 1 PMA approval

OPS Center (for Mobia Medical Inc.) is registered with the FDA (registration 3030239420) in Minneapolis, MN, United States. It lists 2 device types. The FDA files 1 PMA approval under its listings, the newest dated August 27, 2021. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3030239420
Address
5155 East River Road Ste 409, Minneapolis, MN, United States, 55421
Owner or operator
Mobia Medical Inc. (10082738)
Roles
Complaint file establishment, Manufacturer
First device listed
October 7, 2021
Registered through
2026
Brand names listed
MicroTransponder Tunneling Tool, Vivistim System

Devices it lists

DeviceProduct codeClassRoleSource
Instrument, Surgical, Non-PoweredHAO1Manufactureraccessdata.fda.gov
Stimulator, Autonomic Nerve, Implanted For Stroke RehabilitationQPY3Complaint file establishment, Manufactureraccessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
August 27, 2021P210007Vivistim® SystemQPY14September 16, 2026accessdata.fda.gov

Compare with other makers

Updated September 16, 2026. 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.