FENIX GROUP SRL

FDA Device Registration & Listing · Citta' Sant' Angelo Pescara, IT · Registration 3011197718

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
3011197718
FEI Number
3011197718
Entity Name
FENIX GROUP SRL
City/State/Country
Citta' Sant' Angelo Pescara, IT
Establishment Address
Strada Lungofino 187, Citta' Sant' Angelo Pescara 65013, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
FENIX GROUP SRL (Owner Number: 10049818)
Owner / Operator Contact Address
via Agostinone, 9, Montesilvano (PE), IT-NOTA 65015, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AKSENSORALL ENDOSPHERE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2015-08-04

Official Correspondent

No official correspondent registered.

US Agent Details

jay mansour Business: Mansour Consulting LLC Email: jay@mansourconsulting.com Phone: (678) 9088180

Related Public Records

Same Entity

FENIX GROUP SRL
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 3011197718. Last updated year: 2026. Please use registration number 3011197718 when referencing this establishment in official correspondence.
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