Coulot Decolletage S A S

FDA Filings

This page includes the latest FDA filings for Coulot Decolletage S A S. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3006217744
• FEI Number: 3006217744
• Name: David Lennarz
• Owner & Operator: COULOT DECOLLETAGE SAS
• Contact Address: 1, RUE NUNGESSER ET COLI ; CHATELLERAULT FR-86 Vienne 86100 FR
• US Agent:
  • David Lennarz
  • Registrar Corp
  • 757 2240177
  • 757 2240179
  • david.lennarz@registrarcorp.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 144 Research Drive ; Hampton, VA 23666 US
• Establishment Type:
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K181350 | NKG David Lennarz [COULOT DECOLLETAGE SAS]	ASTRA-OCT Spine System	2018-09-19
PMN K181350 | KWP David Lennarz [COULOT DECOLLETAGE SAS]	ASTRA-OCT Spine System	2018-09-19
PMN K151277 | HRS David Lennarz [COULOT DECOLLETAGE SAS]	Airlock	2017-05-07
PMN K143523 | HRS David Lennarz [COULOT DECOLLETAGE SAS]	Airlock	2017-05-07
PMN K143229 | HWC David Lennarz [COULOT DECOLLETAGE SAS]	Nexis	2017-05-07
HWE David Lennarz [COULOT DECOLLETAGE SAS]	Novastep	2017-05-07
ODP David Lennarz [COULOT DECOLLETAGE SAS]	SAMARYS	2017-03-07
ODP David Lennarz [COULOT DECOLLETAGE SAS]	PCB Evolution	2017-03-07
PMN K153386 | NKG David Lennarz [COULOT DECOLLETAGE SAS]	PERLA	2017-01-06
PMN K153386 | KWP David Lennarz [COULOT DECOLLETAGE SAS]	PERLA	2017-01-06
PMN K060473 | HRS David Lennarz [COULOT DECOLLETAGE SAS]	TTC Plates	2014-01-30