Erik Van Der Hoeven

FDA Filings

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

FDA Registration(s)
Registration Number3008691737
FEI Number3008691737
NameErik van der Hoeven
Owner & OperatorDaiya Industry Co., Ltd.
Contact Address1125 Koshinden Minami-ku
Okayama JP-33 Okayama 701-0203 JP
Official Correspondent
  • Toshie Akiyama
  • 81-86-2821245-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address5039 88TH AVE SE
MERCER ISLAND, WA 98040 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
Erik van der Hoeven [Daiya Industry Co., Ltd.]
Ultrathin Bunion Fit2012-03-26
Erik van der Hoeven [Daiya Industry Co., Ltd.]
Ultrathin Bunion Corrector2012-03-26
Erik van der Hoeven [Daiya Industry Co., Ltd.]
Cinderella2012-03-26
Erik van der Hoeven [Daiya Industry Co., Ltd.]
BunionETTE2012-03-26
Erik van der Hoeven [Daiya Industry Co., Ltd.]
BunionBootie2012-03-26

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