US/SS/GS System

GUDID 08800000900926

Osstem Implant Co., Ltd.

Dental implant suprastructure, permanent, preformed
Primary Device ID08800000900926
NIH Device Record Key65c2e936-76cb-4e43-a5e0-afada984429b
Commercial Distribution StatusIn Commercial Distribution
Brand NameUS/SS/GS System
Version Model NumberGSFAM4015NWH
Company DUNS689051793
Company NameOsstem Implant 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 Numbertrue
Manufacturing Datetrue
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
GS108800000900926 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800000900926]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2015-09-23

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08800000907659CAR514NWH
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08800000907635CAR514WH
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08800000907611CAR515N
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08800000907598CAR515NWH
08800000907581CAR515TH
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08800000907567CAR517
08800000907550CAR517N
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08800000907444CAR525
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08800000907420CAR525NTH
08800000907413CAR525NWH
08800000907406CAR525TH
08800000907390CAR525WH
08800000907383CAR527
08800000907376CAR527N

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