Angled Abutment

GUDID 08809955235282

ARUM DENTISTRY 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

Primary Device ID	08809955235282
NIH Device Record Key	6c68340f-d1b5-48f6-a5e9-4b1ab610f278
Commercial Distribution Status	In Commercial Distribution
Brand Name	Angled Abutment
Version Model Number	SAAH452BRP
Company DUNS	557821945
Company Name	ARUM DENTISTRY Co., Ltd.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
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	08809955235282 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K232560

FDA Product Code

NHA	Abutment, Implant, Dental, Endosseous