FDA.reportPublic FDA data

ZrGEN Abutment

Primary DI
08809708759454
Brand
ZrGEN Abutment
Company
Megagen Implant Co. Ltd
Model
ARZXM5016N
Catalog number
ARZXM5016NL
Device description
XPEED AnyRidge Internal Implant System Ø5/ C=0.6/ P=6/ Non-Hex/ Core4
Published
2023-06-22
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
MR Conditional
Rx
true
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
NHAAbutment, Implant, Dental, Endosseous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NHAAbutment, Implant, Dental, EndosseousDental2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K220562000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K220562000TiGEN Abutment, ZrGEN Abutment and Scan Healing AbutmentMegagen Implant Co., Ltd.2022-11-10NHA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08809708759454PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08809708759454088097087594548809708759454

GMDN Terms#

Term, Definition table
TermDefinition
Dental implant suprastructure, permanent, preformedA prefabricated device intended to provide a permanent intermediate fixture level between a dental implant and the final prosthesis/restoration (e.g., bridge, single tooth, overdenture). It includes one or more structural component(s) [e.g., abutment, ball, bar, bar overlay, coping, ring], and may be made of various materials [e.g., titanium (Ti), plastic, gold alloy]. It includes devices glued to prostheses and/or devices that can be replaced during cleaning cycles. An abutment screw(s) may be included, however the suprastructure does not represent the screw(s) in isolation. It may also be referred to as an abutment assembly or mesostructure.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
687388178
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08806388226221BCP EAGLE EYEMGSB0802MGSB08022015-06-29
08806388226238BCP EAGLE EYEMGSB0805MGSB08052015-06-29
08806388226245BCP EAGLE EYEMGSB0810MGSB08102015-06-29
08806388226252BCP EAGLE EYEMGSB0820MGSB08202015-06-29
08806388271504Mega-Oss BovineTMIOSG025IOSG0252018-10-15
08806388271511Mega-Oss BovineTMIOSG050IOSG0502018-10-15
08806388271528Mega-Oss BovineTMIOSG100IOSG1002018-10-15
08806388271535Mega-Oss BovineTMIOSG200IOSG2002018-10-15
08806388271542Mega-Oss BovineTMIOSG500IOSG5002018-10-15
08806388271559Mega-Oss BovineTMIOLG050IOLG0502018-10-15
08806388271566Mega-Oss BovineTMIOLG100IOLG1002018-10-15
08806388271573Mega-Oss BovineTMIOLG200IOLG2002018-10-15
08809977452445BLUEDIAMOND IMPLANTBDC410506C2026-09-04
08809977452469BLUEDIAMOND IMPLANTBDC410506DC2026-09-04
08809977452568BLUEDIAMOND IMPLANTBDC410706C2026-09-04
08809977452582BLUEDIAMOND IMPLANTBDC410706DC2026-09-04
08809977452681BLUEDIAMOND IMPLANTBDC410904C2026-09-04
08809977452704BLUEDIAMOND IMPLANTBDC410904DC2026-09-04
08809977452728BLUEDIAMOND IMPLANTBDC410906C2026-09-04
08809977452742BLUEDIAMOND IMPLANTBDC410906DC2026-09-04

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Primary DI, Brand, Company table
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