Ndx Pacific

FDA Filings

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

FDA Registration(s)
Registration Number3006996325
FEI Number3006996325
NameNDXPacific
Owner & OperatorNDX Pacific
Contact Address1601 Sepulveda Blvd. #628
Manhattan Beach CA 90266 US
Official Correspondent
  • Charles Stapleton
  • x-310-9159121-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address1601 N. Sepulveda Blvd. No. 628
Manhattan Beach, CA 90266 US
Establishment Type
  • Develop Specifications But Do Not Manufacture At This Facility
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
NDXPacific [NDX Pacific]
Biotenta Customized Abutment - Titanium2017-02-06
NDXPacific [NDX Pacific]
Biotenta Customized Abutment - Hybrid2017-02-06
NDXPacific [NDX Pacific]
Restoration, porcelain-fused-to-metal2008-12-12
NDXPacific [NDX Pacific]
Restoration, resin, crown and bridge2008-12-12
NDXPacific [NDX Pacific]
Dentures, full2008-12-12
NDXPacific [NDX Pacific]
Dentures, partial2008-12-12

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