SOLO PACE INC

FDA Device Registration & Listing · Brooklyn Park, MN, US · Registration 3035372913

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
3035372913
FEI Number
3035372913
Entity Name
SOLO PACE INC
City/State/Country
Brooklyn Park, MN, US
Establishment Address
7125 Northland Ter N, Brooklyn Park, MN 55428, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Solo Pace Inc (Owner Number: 10092533)
Owner / Operator Contact Address
7125 Northland Terrace North, Brooklyn Park, MN 55428, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Solo Pace Control

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DTE Pulse-Generator, Pacemaker, External Cardiovascular Class 2 870.3600 2025-01-17

Official Correspondent

Michelle Straight

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Solo Pace Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035372913. Last updated year: 2026. Please use registration number 3035372913 when referencing this establishment in official correspondence.
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