DYNAPULSE MEDICAL LLC

FDA Device Registration & Listing · Minnetonka, MN, US · Registration 3027718340

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
3027718340
FEI Number
3027718340
Entity Name
DYNAPULSE MEDICAL LLC
City/State/Country
Minnetonka, MN, US
Establishment Address
13500 Wayzata Blvd., Minnetonka, MN 55305, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
DynaPulse Medical LLC (Owner Number: 10088485)
Owner / Operator Contact Address
13500 Wayzata Blvd., Minnetonka, MN 55305, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K141919
PMA Number
N/A

All Registered Proprietary Names

Veinoplus Veinoplus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2025-01-22
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2025-01-22
GXY Electrode, Cutaneous Neurology Class 2 882.1320 2025-01-22
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2025-01-22

Official Correspondent

Steffen Magnell

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K122948 Gemore Technology Co, Ltd. GEM-STIM COMBO STIMULATOR 2012-12-21
K033455 Biomedical Life Systems, Inc. ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5 2004-01-15
K810593 Medical Devices, Inc. NEUROPAC ULTRA I 1981-03-13
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027718340. Last updated year: 2026. Please use registration number 3027718340 when referencing this establishment in official correspondence.
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