Lorena Trabucco

FDA Filings

This page includes the latest FDA filings for Lorena Trabucco. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number9614846
FEI Number3005404334
NameLorena Trabucco
Owner & OperatorHERNIAMESH SRL
Contact Address540 MUTTONTOWN EASTWOODS ROAD
Syosset NY 11791 US
Official Correspondent
  • LORENA TRABUCCO
  • 01-516-9879364-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address540 Muttontown Eastwoods Rd
Syosset, NY 11791 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Lorena Trabucco [HERNIAMESH SRL]
Aiartex, Aiartex Plus, Aiartex PM, Aiartex Pillow2012-01-17
Lorena Trabucco [HERNIAMESH SRL]
Aiartex, Aiartex PM, Aiartex Pillow2012-01-17
Lorena Trabucco [HERNIAMESH SRL]
Quadriaxial Mesh2009-01-02
Lorena Trabucco [HERNIAMESH SRL]
Hertra, Hertra 2, Hertra 2A, Hermesh, Plug T1, Plug T2, Plug T3, Plug T4, T5, Net Plug & Patch, Round Patch, Oval Patch,2009-01-02
Lorena Trabucco [HERNIAMESH SRL]
Colostomy Patch, Hertra Kits2009-01-02
Lorena Trabucco [HERNIAMESH SRL]
Relimesh2009-01-02
Lorena Trabucco [HERNIAMESH SRL]
Hermesh 72009-01-02
Lorena Trabucco [HERNIAMESH SRL]
T-Sling2009-01-02

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