Vortex Surgical

FDA Filings

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

FDA Registration(s)

• Registration Number: 3013002167
• FEI Number: 3013002167
• Name: Vortex Surgical
• Owner & Operator: Vortex Surgical
• Contact Address: 1185 Lakewood Drive ; Pacific MO 63069 US
• Official Correspondent:
  • Pamela G Boone
  • 001-314-9739172-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 680 Crown Industrial Ct Ste F ; Chesterfield, MO 63005 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K191846 | HQB Vortex Surgical	Laser Probes	2020-01-22
HNX Vortex Surgical	Todorich Illuminated Depressor (TID)	2019-08-23
HNR Vortex Surgical	ACTU8 Forceps	2018-03-09
KDD Vortex Surgical	Injection Kits	2016-11-30
MXY Vortex Surgical	Soft Tip Cannula	2016-11-28
HNQ Vortex Surgical	Edge Advantage ILM Elevator	2016-11-28
HMX Vortex Surgical	Soft Tip Cannula	2016-11-28

Similar & Related FDA Registered Companies

• Vortex Surgical Inc
• VORTEX SURGICAL, LLC