Transenterix Italia S R L

FDA Filings

This page includes the latest FDA filings for Transenterix Italia S R L. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3012880598
FEI Number3012880598
NameTransEnterix Italia, S. r. L
Owner & OperatorTransEnterix, Inc.
Contact Address635 Davis Drive Suite 300
Morrisville NC 27560 US
Official Correspondent
  • Stephanie Fullard
  • x-919-7658000-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressViale dell'Innovazione 3
Milano Lombardia, 20126 IT
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
TransEnterix Italia, S. r. L [TransEnterix, Inc.]
Senhance Ultrasonic System2019-01-18
TransEnterix Italia, S. r. L [TransEnterix, Inc.]
Senhance Surgical System2017-11-06
TransEnterix Italia, S. r. L [TransEnterix, Inc.]
Senhance Surgical System2017-11-06

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