Clerad

FDA Filings

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

FDA Registration(s)

• Registration Number: 3009518669
• FEI Number: 3009518669
• Name: Rick Kilgus
• Owner & Operator: CLERAD
• Contact Address: 15 rue Patrick Depailler ; Clermont-Ferrand FR-63 Puy-de-Dome 63000 FR
• Official Correspondent:
  • Philippe BRETTE
  • 033-4-73746240-x
• US Agent:
  • Rick Kilgus
  • minvasive surgical
  • 401 2892223
  • 401 2892813
  • r.kilgus@minvasivesurgical.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 327 Water Street ; Warren, RI 02885 US
• Establishment Type: Manufacture Medical Device

• Registration Number: 3010883036
• FEI Number: 3010883036
• Name: CLERAD LLC
• Owner & Operator: CLERAD
• Contact Address: 15 rue Patrick Depailler ; Clermont-Ferrand FR-63 Puy-de-Dome 63000 FR
• Official Correspondent:
  • Philippe BRETTE
  • 033-4-73746240-x
• Registration Status: 1
• Initial Importer: Y
• Registration Expiration: 2020-04-25
• Registration Address: 362 Broadway ; Providence, RI 02909 US

FDA Filings

Device Company	Device	Date
IZD Rick Kilgus [CLERAD]	KUBTEC GammaPRO	2012-09-07
IZD Rick Kilgus [CLERAD]	GAMMA SUP II	2012-09-07