SNUCONE BONE LEVEL IMPLANT SYSTEM

GUDID 08800020845702

SNUCONE Co.,LTD.

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed
Primary Device ID08800020845702
NIH Device Record Key0926ee9b-7e01-40ff-9d2e-f05e7f73e65b
Commercial Distribution StatusIn Commercial Distribution
Brand NameSNUCONE BONE LEVEL IMPLANT SYSTEM
Version Model NumberACAMR-45315-FA
Company DUNS688806132
Company NameSNUCONE Co.,LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108800020845702 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


[08800020845702]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-01
Device Publish Date2023-02-21

On-Brand Devices [SNUCONE BONE LEVEL IMPLANT SYSTEM]

08800020854964AF+B-6814S
08800020854957AF+B-6813S
08800020854940AF+B-6812S
08800020854933AF+B-6811S
08800020854926AF+B-6810S
08800020854919AF+B-6809S
08800020854902AF+B-6808S
08800020854896AF+B-6807S
08800020854889AF+B-6314S
08800020854872AF+B-6313S
08800020854865AF+B-6312S
08800020854858AF+B-6311S
08800020854841AF+B-6310S
08800020854834AF+B-6309S
08800020854827AF+B-6308S
08800020854810AF+B-6307S
08800020854803AF+B-5814S
08800020854797AF+B-5813S
08800020854780AF+B-5812S
08800020854773AF+B-5811S
08800020854766AF+B-5810S
08800020854759AF+B-5809S
08800020854742AF+B-5808S
08800020854735AF+B-5807S
08800020854728AF+B-5314S
08800020854711AF+B-5313S
08800020854704AF+B-5312S
08800020854698AF+B-5311S
08800020854681AF+B-5310S
08800020854674AF+B-5309S
08800020854667AF+B-5308S
08800020854650AF+B-5307S
08800020854643AF+B-4814S
08800020854636AF+B-4813S
08800020854629AF+B-4812S
08800020854612AF+B-4811S
08800020854605AF+B-4810S
08800020854599AF+B-4809S
08800020854568AF+B-4314S
08800020854551AF+B-4313S
08800020854544AF+B-4312S
08800020854537AF+B-4311S
08800020854513AF+B-4309S
08800020854483AF+B-4014S
08800020854476AF+B-4013S
08800020854452AF+B-4011S
08800020854438AF+B-4009S
08800020854414AF+B-4007S
08800020854407AF+B-3514S
08800020854391AF+B-3513S

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.