Mobia Medical Inc.

FDA Device Registration & Listing · Austin, TX, US · Registration 3012309950

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
3012309950
FEI Number
3012309950
Entity Name
Mobia Medical Inc.
City/State/Country
Austin, TX, US
Establishment Address
2802 Flintrock Trace #226, Austin, TX 78738, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
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
P210007

All Registered Proprietary Names

Vivistim System

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

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
3030239420 OPS Center (for Mobia Medical Inc.) Minneapolis, MN, US

Similar Registrations

Registration Number Establishment Name Location
3030239420 OPS Center (for Mobia Medical Inc.) Minneapolis, MN, US
2030624 Isomedix Operations, Inc. Temecula, CA, US
3010326622 Centro de Construccion de Cardioestimuladores del Uruguay S.A. Montevideo, UY
2032521 PRO-TECH DESIGN & MFG., INC. SANTA FE SPRINGS, CA, US
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 3012309950. Last updated year: 2026. Please use registration number 3012309950 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.