Bone Cup

GUDID 08800036261312

Biotem Co., ltd

Dental implant system
Primary Device ID08800036261312
NIH Device Record Key2eaf0cb1-76ad-451d-84da-ccbaac0f12db
Commercial Distribution StatusIn Commercial Distribution
Brand NameBone Cup
Version Model NumberBPC07D20
Company DUNS557793214
Company NameBiotem Co., ltd
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800036261312 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


[08800036261312]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-08-26
Device Publish Date2025-08-18

On-Brand Devices [Bone Cup]

08800036261343BPC10D20
08800036261336BPC09D20
08800036261329BPC08D20
08800036261312BPC07D20
08800036261305BPC06D20

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.