Vita North America

FDA Filings

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

Vita North America holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

• Lindsay Tilton
• Kyle Uyemura

FDA Registration(s)

• Registration Number: 2082832
• FEI Number: 2082832
• Name: VITA North America
• Owner & Operator: VITA North America
• Contact Address: 22705 Savi Ranch Parkway, Suite 100 --; Yorba Linda CA 92887 US
• Official Correspondent:
  • Lindsay Tilton
  • x-925-6999091-x
• Registration Status: 1
• Initial Importer: Y
• Registration Expiration: 2020-04-25
• Registration Address: 22705 Savi Ranch Parkway Ste 100 ; Yorba Linda, CA 92887 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
EGD VITA North America	Vionic Wax	2020-03-02
PMN K191926 | EBI VITA North America	Vionic bond	2020-02-19
ELM VITA North America	Vionic Teeth	2020-02-19

U.S. Import Records [external site]

Import ID	Shipment	Cargo Description	Quantity
2018123132358	Anvers,Belgium -> Los Angeles, California	DENTAL PRODUCTS HS CODE 392310	53 PCS
2018070210860	Genova,Italy -> Long Beach, California	POLYURETHANE RESIN	26 PCS