Agustin Turriza

FDA Filings

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

FDA Registration(s)

• Registration Number: 3009401905
• FEI Number: 3009401905
• Name: Agustin Turriza
• Owner & Operator: ADROIT MANUFACTURING CO.
• Contact Address: Plot No: 138 Dist. Valsad; Umbergaon IN-GJ Gujarat 396171 IN
• US Agent:
  • Agustin Turriza
  • Spectra Medical Devices, Inc.
  • 978 6570889
  • 978 6574339
  • aturriza@spectramedical.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 260H Fordham Rd ; Wilmington, MA 01887 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
MDM Agustin Turriza [ADROIT MANUFACTURING CO.]	Tunneler	2012-04-03
MDM Agustin Turriza [ADROIT MANUFACTURING CO.]	Trocar	2012-04-03

Similar & Related FDA Registered Companies

• Spectra Medical Devices, Inc.