Hoya Corp Pentax Friedberg Factory

FDA Filings

This page includes the latest FDA filings for Hoya Corp Pentax Friedberg Factory. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3013956442
• FEI Number: 3013956442
• Name: HOYA Corporation PENTAX Friedberg Factory
• Owner & Operator: HOYA Corporation PENTAX Division
• Contact Address: 3 Paragon Drive ; Montvale NJ 07645 US
• Official Correspondent:
  • William Goeller
  • x-201-5712318-x
• US Agent:
  • William Goeller
  • HOYA CORPORATION PENTAX DIVISION
  • 201 5712318
  • 201 5712340
  • william.goeller@pentaxmedical.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Paul-Lenz-Strasse 5 ; Friedberg Bayern, 86316 DE
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K171011 | EOB HOYA Corporation PENTAX Friedberg Factory [HOYA Corporation PENTAX Division]	VIDEO PROCESSOR (CP-1000)	2018-09-11
PMN K171011 | EOB HOYA Corporation PENTAX Friedberg Factory [HOYA Corporation PENTAX Division]	VIDEO NASOPHARYNGOLARYNGOSCOPE (VNL9-CP)	2018-09-11