IU Healing Abutment

GUDID 08800026102267

WARANTEC.Co.,Ltd

Dental implant system
Primary Device ID08800026102267
NIH Device Record Key44d16c0d-3016-490d-9442-c5c67e6c7dcd
Commercial Distribution StatusIn Commercial Distribution
Brand NameIU Healing Abutment
Version Model NumberIUHA4010A
Company DUNS688857820
Company NameWARANTEC.Co.,Ltd
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800026102267 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-20
Device Publish Date2023-04-12

On-Brand Devices [IU Healing Abutment]

08800026106036IUHA6060
08800026102533IUHA6050
08800026102526IUHA6040
08800026102519IUHA6030
08800026102502IUHA6020
08800026102496IUHA6010
08800026102489IUHA5060
08800026102472IUHA5050
08800026102465IUHA5040
08800026102458IUHA5030
08800026102441IUHA5020
08800026102434IUHA5010
08800026102427IUHA4060
08800026102410IUHA4050
08800026102403IUHA4040
08800026102397IUHA4030
08800026102380IUHA4020
08800026102373IUHA4010
08800026102366IUHA5060A
08800026102359IUHA5050A
08800026102342IUHA5040A
08800026102335IUHA5030A
08800026102328IUHA5020A
08800026102311IUHA5010A
08800026102304IUHA4060A
08800026102298IUHA4050A
08800026102281IUHA4040A
08800026102274IUHA4030A
08800026102267IUHA4010A
08800026102243IUHA4020A

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