Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012170108

FEI Number

3012170108

Entity Name

JET TECH EUROPE S.R.L.

City/State/Country

Milan Milano, IT

Establishment Address

Via Giovanni Silvestri, 15, Milan Milano 20126, IT

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device,Foreign Private Label Distributor

Owner / Operator

Jet Tech Europe S.r.l. (Owner Number: 10080192)

Owner / Operator Contact Address

Via Giovanni Silvestri, 15, Milan, IT-MI 20126, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MESOJET HY-PO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GFE	Brush, Dermabrasion, Powered	General, Plastic Surgery	Class 1	878.4820	2021-01-18

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

Jet Tech Europe S.r.l.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

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3012616488	BRERA MEDICAL INCORPORATED	Northborough, MA, US
3029972466	ASTERASYS CO., LTD.	Seongdong-gu Seoul, KR
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012170108. Last updated year: 2026. Please use registration number 3012170108 when referencing this establishment in official correspondence.