FDA Registration Number: 3008494722

Last Validated: October 19, 2021

Status: Valid

Valid2021 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  
Implant, Endosseous, Root-Form DZE Valid October 18, 2021

Device Listing

Device Name

Implant, Endosseous, Root-Form

Product Code

DZE

Company Function(s)

Specification Developer

Proprietary Name(s)

Implant, Endosseous, Root-Form DZE Valid October 18, 2021

Device Listing

Device Name

Implant, Endosseous, Root-Form

Product Code

DZE

Company Function(s)

Specification Developer

Proprietary Name(s)

Implant, Endosseous, Root-Form DZE Valid October 18, 2021

Device Listing

Device Name

Implant, Endosseous, Root-Form

Product Code

DZE

Company Function(s)

Specification Developer

Proprietary Name(s)

Implant, Endosseous, Root-Form DZE Valid October 18, 2021

Device Listing

Device Name

Implant, Endosseous, Root-Form

Product Code

DZE

Company Function(s)

Specification Developer

Proprietary Name(s)

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