Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005699251

FEI Number

3005699251

Entity Name

PASINI LABORATORIO CHIMICO S.N.C.

City/State/Country

Burago Di Molgora Lombardy, IT

Establishment Address

Via dell'Industria, 5, Burago Di Molgora Lombardy 20875, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Pasini Laboratorio Chimico S.n.c. (Owner Number: 10062804)

Owner / Operator Contact Address

Via dell'Industria, 5, Burago Di Molgora, IT-NOTA 20875, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

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
KOO	Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt	Dental	Class 1	872.3490	2020-03-09
KOQ	Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)	Dental	Class 1	872.3410	2020-03-09

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Pasini Laboratorio Chimico S.n.c.

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 3005699251. Last updated year: 2026. Please use registration number 3005699251 when referencing this establishment in official correspondence.