Laura Nea

FDA Filings

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

FDA Registration(s)

• Registration Number: 3003402518
• FEI Number: 3003402518
• Name: Laura Nea
• Owner & Operator: Tecan Group AG
• Contact Address: 103 Seestrasse --; Maennedorf CH-ZH Zurich 8708 CH
• Official Correspondent:
  • Claudia Solimeo Meneghisse
  • 41-044-922-8992
• US Agent:
  • Laura Nea
  • TECAN U.S.
  • 919 3615200 19524
  • 919 3615201
  • REGULATORY.AFFAIRS.US@TECAN.COM
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 9401 Globe Center Drive Suite No. 140; Morrisville, NC 27560 US
• Establishment Type:
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device Company	Device	Date
JJF Laura Nea [Tecan Group AG]	Freedom EVOlyzer	2008-01-17
KPA Laura Nea [Tecan Group AG]	PROFI BLOT T48	2005-02-23
KPA Laura Nea [Tecan Group AG]	PROFI BLOT 48	2005-02-23
KPA Laura Nea [Tecan Group AG]	PROFI BLOT 48-2in1	2005-02-23
JJE Laura Nea [Tecan Group AG]	Freedom EVOlyzer	2005-02-22
JQW Laura Nea [Tecan Group AG]	Genesis FE 500 :	2001-11-06
JQW Laura Nea [Tecan Group AG]	Freedom EVOlyzer :	2001-11-06
JQW Laura Nea [Tecan Group AG]	Freedom EVO Clinical :	2001-11-06
JQW Laura Nea [Tecan Group AG]	Freedom EVO :	2001-11-06
JQW Laura Nea [Tecan Group AG]	Freedom EVO 75 :	2001-11-06
JQW Laura Nea [Tecan Group AG]	Fluent	2001-11-06

Similar & Related FDA Registered Companies

• TECAN U.S.
• TECAN US