FDA.reportPublic FDA data

Osteon Medical

Primary DI
D102BAR0
Brand
Osteon Medical
Company
IMPLANT SOLUTIONS PTY LTD
Model
1
Device description
The Osteon Precision Milled Suprastructure is indicated for attachment to dental abutments in the treatment of partially or fully edentulous jaws for the purpose of restoring chewing function. The Osteon Precision Milled Suprastructures are intended for attachment to a minimum of two (2) abutments.
Published
2022-07-26
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
NHAAbutment, Implant, Dental, Endosseous
NSKDentures, Partial
NSLDentures, Full
NSMRestoration, Resin
NSNRestoration, Resin, Crown And Bridge
NSPRestoration, Porcelain
NSQRestoration, Base Metal

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NHAAbutment, Implant, Dental, EndosseousDental2
NSKDentures, PartialUnknownN
NSLDentures, FullUnknownN
NSMRestoration, ResinUnknownN
NSNRestoration, Resin, Crown And BridgeUnknownN
NSPRestoration, PorcelainUnknownN
NSQRestoration, Base MetalUnknownN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
D102BAR0PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Dental implant suprastructure, permanent, custom-madeA custom-made device intended to provide a permanent intermediate fixture level between a dental implant and the final prosthesis/restoration (e.g., bridge, single tooth, overdenture). It includes one or more structural component(s) [e.g., abutment, ball, bar, bar overlay, coping], and may be made of various materials [e.g., titanium (Ti), plastic, gold alloy]; an abutment screw(s) may be included, however the suprastructure does not represent the screw(s) in isolation. It may also be referred to as an abutment assembly or mesostructure and is manufactured for a specific patient.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+61392640111info@osteonmedical.com

Regulatory Flags#

DUNS number
756242111
Device count
1
Premarket exempt
true
Serial number
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
D102SGKAA0Osteon Medical12022-12-19
D102SGKBC0Osteon Medical12022-12-19
D102SGKBD0Osteon Medical12022-12-19
D102SGKBF20Osteon Medical12024-02-05
D102SGKBG20Osteon Medical12024-02-05
D102SGKBE20Osteon Medical12023-09-11
D102SGKAA20Osteon Medical12022-10-24
D102SCANGAUGEKIT0Osteon Medical12022-07-26
D102BARNIOSV10Osteon Medical12023-01-19
D102BARNIOSV20Osteon Medical12023-01-19
D102BARNIOSV30Osteon Medical12023-01-19
D102BARNIOSV40Osteon Medical12023-01-19
D102BRIDGE0Osteon Medical12022-07-26

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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