5444-0-500

GUDID 07613252133551

CMF CUSTOMIZED IMPLANT KIT MIDFACE

Howmedica Osteonics Corp.

Cranioplasty plate, non-alterable
Primary Device ID07613252133551
NIH Device Record Keydc6fbf42-888a-437a-b2a6-f0b2a25d1d81
Commercial Distribution StatusIn Commercial Distribution
Version Model Number5444-0-500
Catalog Number5444-0-500
Company DUNS058311945
Company NameHowmedica Osteonics Corp.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107613252133551 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KKYMATERIAL, POLYTETRAFLUOROETHYLENE VITREOUS CARBON, FOR MAXILLOFACIAL RECONSTRUCTION

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-24

Devices Manufactured by Howmedica Osteonics Corp.

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07613327296990 - Trident X3 Insert2026-01-29 Trident X3 0 Degree Polyethylene Insert
07613327297027 - Trident X3 Insert2026-01-29 Trident X3 0 Degree Polyethylene Insert
07613327297041 - Trident X3 Insert2026-01-29 Trident X3 0 Degree Polyethylene Insert
07613327297058 - Trident X3 Insert2026-01-29 Trident X3 0 Degree Polyethylene Insert
07613327297065 - Trident X3 Insert2026-01-29 Trident X3 0 Degree Polyethylene Insert
07613327338751 - Trident X3 Insert2026-01-29 Trident X3 10 Degree Polyethylene Insert

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