Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010290186

FEI Number

3010290186

Entity Name

TOSKANI

City/State/Country

Barcelona, ES

Establishment Address

Ptje. Ciutadans 4, Barcelona 08005, ES

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Toskani (Owner Number: 10090033)

Owner / Operator Contact Address

Ptje. Ciutadans 4, Barcelona, ES-B 08005, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K180778

PMA Number

N/A

All Registered Proprietary Names

TKN MesojectGun MTDerm TOSKANIMED

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	2025-12-02
QAI	Powered Microneedle Device	General, Plastic Surgery	Class 2	878.4430	2024-02-06

Official Correspondent

Iwona Duda

US Agent Details

Roberta Baldini Business: Toskani USA Corporation Email: roberta.baldini@toskani.us Phone: (954) 8047910

Related Public Records

Same Entity

Toskani

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 3010290186. Last updated year: 2026. Please use registration number 3010290186 when referencing this establishment in official correspondence.