Collimare L L C

FDA Filings

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

FDA Registration(s)

• Registration Number: 3007137304
• FEI Number: 3007137304
• Name: COLLIMARE, LLC
• Owner & Operator: Collimare, LLC
• Contact Address: 13401 W 43RD DR STE 7; Golden CO 80403 US
• Official Correspondent:
  • Howard C Thomas
  • 1-303-2781496-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 13401 W 43rd Dr Ste 7 ; Golden, CO 80403 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 00862005000368 COLLIMARE, LLC	Collimare	2018-07-06
GUDID 00862005000351 COLLIMARE, LLC	Collimare	2018-07-06
GUDID 00862005000344 COLLIMARE, LLC	Collimare	2018-07-06
GUDID 00862005000337 COLLIMARE, LLC	Collimare	2018-07-06
GUDID 00862005000320 COLLIMARE, LLC	Collimare	2018-07-06
GUDID 00862005000313 COLLIMARE, LLC	Collimare	2018-07-06
GUDID 00862005000306 COLLIMARE, LLC	Collimare	2018-07-06
PMN K073124 | IZX COLLIMARE, LLC	Collimare	2008-06-06
PMN K073124 | IZW COLLIMARE, LLC	Collimare	2008-06-06
PMN K073124 COLLIMARE, LLC	COLLIMARE COLLIMATOR FAMILY	2007-11-16