MOVEO SRL

FDA Device Registration & Listing · Padova, IT · Registration 3030490678

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
3030490678
FEI Number
3030490678
Entity Name
MOVEO SRL
City/State/Country
Padova, IT
Establishment Address
Via Monsignor Giovanni Fortin, number 38, Padova 35128, IT
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Moveo Srl (Owner Number: 10090028)
Owner / Operator Contact Address
Via Monsignor Giovanni Fortin, number 38, Padova, IT-PD 35128, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ExoAnkle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITW Joint, Ankle, External Brace Physical Medicine Class 1 890.3475 2024-06-24

Official Correspondent

Fausto Panizzolo

US Agent Details

Scott Bednar Business: QA/RA CONSULTING GROUP, INC. Email: sbednar@qaraconsultinggroup.com Phone: (412) 4188066

Related Public Records

Same Entity

Moveo Srl
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030490678. Last updated year: 2026. Please use registration number 3030490678 when referencing this establishment in official correspondence.
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