Hinai Watch Works Hinai Plant

FDA Filings

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

FDA Registration(s)
Registration Number3010316851
FEI Number3010316851
NameHINAI WATCH-WORKS, Hinai 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 Address69-3 Nobiraki, Niidate, Hinai-machi
Odate-shi Akita, 018-5712 JP
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
HINAI WATCH-WORKS, Hinai Plant [HOYA Corporation PENTAX Division]
LH-150PC LIGHT SOURCE (LH-150PC)2006-01-04
HINAI WATCH-WORKS, Hinai Plant [HOYA Corporation PENTAX Division]
LH-150PC BUNDLE (LH-150PC-US-ENT )2006-01-04
HINAI WATCH-WORKS, Hinai Plant [HOYA Corporation PENTAX Division]
LAMP KIT, LH-150PC (OL-H4)2006-01-04
HINAI WATCH-WORKS, Hinai Plant [HOYA Corporation PENTAX Division]
ADAPTER PORT, SCOPE TO LIGHT SOURCE (OL-H3)2006-01-04

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