FDA Registration Number: 3008494722

Last Validated: November 27, 2022

Status: Valid

Valid2023 U.S. FDA Medical Device Establishment Registration

Osseofuse International Inc.

Establishment Information

6170 West Desert Inn Rd.
Suite B
Las Vegas NV, US

Official Correspondent

Registrar Corp
144 Research Drive
Hampton VA, USA 23666
Registration of a device establishment, assignment of a registration number, or listing of a medical device does not in any way denote approval of the establishment or its products by U.S. FDA.

Listings on file with FDA

Device Name Product Code Status Last Validated  
Abutment, Implant, Dental, Endosseous NHA Valid November 26, 2022

Device Listing

Device Name

Abutment, Implant, Dental, Endosseous

Product Code

NHA

Company Function(s)

Specification Developer

Proprietary Name(s)

Abutment, Implant, Dental, Endosseous NHA Valid November 26, 2022

Device Listing

Device Name

Abutment, Implant, Dental, Endosseous

Product Code

NHA

Company Function(s)

Specification Developer

Proprietary Name(s)

Implant, Endosseous, Root-Form DZE Valid November 26, 2022

Device Listing

Device Name

Implant, Endosseous, Root-Form

Product Code

DZE

Company Function(s)

Specification Developer

Proprietary Name(s)

Abutment, Implant, Dental, Endosseous NHA Valid November 26, 2022

Device Listing

Device Name

Abutment, Implant, Dental, Endosseous

Product Code

NHA

Company Function(s)

Specification Developer

Proprietary Name(s)

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