Impression Coping Driver

GUDID 08800011265267

POINTIMPLANT Co., Ltd.

Surgical screwdriver, reusable
Primary Device ID08800011265267
NIH Device Record Keydcfd0578-378d-488e-ae3f-ce49498dd89c
Commercial Distribution StatusIn Commercial Distribution
Brand NameImpression Coping Driver
Version Model NumberOBICDL
Company DUNS695333960
Company NamePOINTIMPLANT Co., Ltd.
Device Count1
DM Exemptfalse
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 Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800011260804 [Previous]
GS108800011265267 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


[08800011265267]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-08-01
Device Publish Date2025-07-24

On-Brand Devices [Impression Coping Driver]

08800011265304OBICDLP
08800011265298OBICDSP
08800011265267OBICDL

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