WIEMSPRO S.L

FDA Device Registration & Listing · Malaga, ES · Registration 3015781781

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
3015781781
FEI Number
3015781781
Entity Name
WIEMSPRO S.L
City/State/Country
Malaga, ES
Establishment Address
Jacinto Verdaguer, 11, Malaga 29002, ES
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Wiemspro S.L (Owner Number: 10061109)
Owner / Operator Contact Address
Jacinto Verdaguer, 11, Malaga, ES-MA 29002, ES
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K181955
PMA Number
N/A

All Registered Proprietary Names

Wiemspro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2019-08-22

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Wiemspro S.L
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
K221200 Xbody Hungary Kft. XBody Go USA, XBody Pro USA 2023-01-31

Similar Registrations

Registration Number Establishment Name Location
3015282440 MEDICAL CABLES S.L. Malaga, ES
3029924973 SHENZHEN SINREL TECH LTD Shenzhen Guangdong, CN
3013889849 Expeditors International of Washington, Inc. Salt Lake City, UT, US
3044675848 PEPPER INTERACTIVE INC Wilmington, DE, US
3016674228 Medical Currents Ltd Dublin, IE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015781781. Last updated year: 2026. Please use registration number 3015781781 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.