DOMPE FARMACEUTICI S.P.A.

FDA Device Registration & Listing · L Aquila Abruzzo, IT · Registration 3004216297

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
3004216297
FEI Number
3004216297
Entity Name
DOMPE FARMACEUTICI S.P.A.
City/State/Country
L Aquila Abruzzo, IT
Establishment Address
Via Campo di Pile, L Aquila Abruzzo 67100, IT
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Dompe farmaceutici S.p.A. (Owner Number: 10057047)
Owner / Operator Contact Address
Via Campo di Pile, L’Aquila, IT-65 67100, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pipette SI5 Sterile Dropper SI6

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2018-05-11

Official Correspondent

No official correspondent registered.

US Agent Details

Jose de la Cruz Business: Dompe US Inc. Email: Jose.Delacruz@dompe.com Phone: (650) 4180795

Related Public Records

Same Entity

Dompe farmaceutici S.p.A.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3017521274 Dompe US, Inc. San Mateo, CA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004216297. Last updated year: 2026. Please use registration number 3004216297 when referencing this establishment in official correspondence.
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