HYDRA SRL

FDA Device Registration & Listing · Mirandola Modena, IT · Registration 3011707889

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
3011707889
FEI Number
3011707889
Entity Name
HYDRA SRL
City/State/Country
Mirandola Modena, IT
Establishment Address
Via Savonarola 4, Mirandola Modena 41037, IT
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Hydra Srl (Owner Number: 10049329)
Owner / Operator Contact Address
Via Savonarola 4, Mirandola, IT-MO 41037, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MUU System, Suction, Lipoplasty General, Plastic Surgery Class 2 878.5040 2023-02-08

Official Correspondent

Antonio Bosetto

US Agent Details

Lorenzo Da Madice Business: ISOPLAN USA Email: isoplan@fda-510k.com Phone: (386) 8680618

Related Public Records

Same Entity

Hydra 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 3011707889. Last updated year: 2026. Please use registration number 3011707889 when referencing this establishment in official correspondence.
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