Magic Cylinder

GUDID 08800039371667

InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)

Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use

Primary Device ID	08800039371667
NIH Device Record Key	7424021d-bca7-4d82-b239-cce836bb035c
Commercial Distribution Status	In Commercial Distribution
Brand Name	Magic Cylinder
Version Model Number	MTCH55
Company DUNS	631169224
Company Name	InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Conditional
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800039371667 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K201621

FDA Product Code

NHA	Abutment, Implant, Dental, Endosseous