FELDI SRL

FDA Device Registration & Listing · Seriate Bergamo, IT · Registration 3025235024

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
3025235024
FEI Number
3025235024
Entity Name
FELDI SRL
City/State/Country
Seriate Bergamo, IT
Establishment Address
Via Perugino, 10, Seriate Bergamo 24068, IT
Establishment Type(s)
Foreign Private Label Distributor
Owner / Operator
Feldi Srl (Owner Number: 10087929)
Owner / Operator Contact Address
Via Perugino, 10, Seriate, IT-BG 24068, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tesmed CELLULITE Tesmed FIT 5.4 Tesmed FIT 5.8 Tesmed TE-880R Plus Tesmed Trio 6.5

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYG Massager, Therapeutic, Manual Physical Medicine Class 1 890.5660 2023-05-03
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2024-03-20
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2024-03-20
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2024-03-20
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2024-03-20
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2024-03-20
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2024-03-20

Official Correspondent

Milena Medolago

US Agent Details

Caterina Zimmerman Business: Pangea Export USA LLC Email: info@pangeaexport.us Phone: (415) 2506061

Related Public Records

Same Entity

Feldi Srl
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
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
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025235024. Last updated year: 2026. Please use registration number 3025235024 when referencing this establishment in official correspondence.
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