OPS Center (for Mobia Medical Inc.)

FDA Device Registration & Listing · Minneapolis, MN, US · Registration 3030239420

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
3030239420
FEI Number
3030239420
Entity Name
OPS Center (for Mobia Medical Inc.)
City/State/Country
Minneapolis, MN, US
Establishment Address
5155 East River Road Ste 409, Minneapolis, MN 55421, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Mobia Medical Inc. (Owner Number: 10082738)
Owner / Operator Contact Address
2802 Flintrock Trace #226, Austin, TX 78738, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Vivistim System MicroTransponder Tunneling Tool

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QPY Stimulator, Autonomic Nerve, Implanted For Stroke Rehabilitation Unknown Class 3 N/A 2021-10-07
HAO Instrument, Surgical, Non-Powered Neurology Class 1 882.4535 2024-07-23

Official Correspondent

W. Brent Tarver

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mobia Medical Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3012309950 Mobia Medical Inc. Austin, TX, US

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3013368220 CIRTEC MEDICAL Brooklyn Park, MN, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030239420. Last updated year: 2026. Please use registration number 3030239420 when referencing this establishment in official correspondence.
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