Yoshikawa Kasei Osaka Plant

FDA Filings

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

FDA Registration(s)
Registration Number3004638277
FEI Number3004638277
NameYOSHIKAWA KASEI OSAKA PLANT
Owner & OperatorHOYA Corporation PENTAX Division
Contact Address3 Paragon Drive
Montvale NJ 07645 US
Official Correspondent
  • William Goeller
  • x-201-5712318-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address56-34 Yokozutsumi, Tsurmi-Ku
Osaka-shi Osaka, 538-0052 JP
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
YOSHIKAWA KASEI OSAKA PLANT [HOYA Corporation PENTAX Division]
HEMOSTASIS FORCEPS, WD2.6, LN2200, QTY 5 (HS-D2622)2017-12-12
YOSHIKAWA KASEI OSAKA PLANT [HOYA Corporation PENTAX Division]
HEMOSTASIS FORCEPS, WD2.6, LN1800, QTY 5 (HS-D2618)2017-12-12

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