SUBLIMED

FDA Device Registration & Listing · Moirans Auvergne-Rhone-Alpes, FR · Registration 3015588280

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
3015588280
FEI Number
3015588280
Entity Name
SUBLIMED
City/State/Country
Moirans Auvergne-Rhone-Alpes, FR
Establishment Address
137 Rue Mayoussard, Moirans Auvergne-Rhone-Alpes 38380, FR
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
SUBLIMED (Owner Number: 10088953)
Owner / Operator Contact Address
137 Rue Mayoussard, Moirans, FR-ARA 38380, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K252767
PMA Number
N/A

All Registered Proprietary Names

actiTENS mini spare actiTENS mini Textile Accessory actiTENS mini KIT actiTENS iOs app actiTENS Android app

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NYN Stimulator, Electrical, Transcutaneous, For Arthritis Neurology Class 2 882.5890 2026-04-24
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2026-04-24
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2026-04-24
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2026-04-24
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2026-04-24

Official Correspondent

Adrien HALLET

US Agent Details

Robert Packard Business: Medical Device Academy Incorporated Email: rob@fdaestar.com Phone: (802) 2581881

Related Public Records

Same Entity

SUBLIMED
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

Similar Registrations

Registration Number Establishment Name Location
3003255790 WITKO INCORPORATED Wolcott, IN, US
3038295706 JUST KEEP HEALTHY CO., LTD. Samkkei Munichay District Kampong Speu, KH
3007731000 VGH SOLUTIONS INC Markham Ontario, CA
3008048783 DRTV Asia LTD Panyu GuangZhou Guangdong, CN
3008507279 CHOICEMMED AMERICA CORPORATION Bristol, PA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015588280. Last updated year: 2026. Please use registration number 3015588280 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.