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Angled Abutment

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref ARIEAAHN50415T

by Megagen Implant Co. Ltd

Identity

Trade Name
Angled Abutment FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Angled Abutment EUDAMED
ARi ExCon Implant System FDA UDI
Model / Reference
ARIEAAHN50415T EUDAMED
ARIEAAHN50415 FDA UDI
ARIEAAHN50515 FDA UDI
Description
ARi ExCon Implant System FDA UDI

Identifiers

Catalog Number
ARIEAAHN50415T FDA UDI
ARIEAAHN50515T FDA UDI
Primary DI / UDI-DI
08809854029555 EUDAMEDFDA UDI
08809854029579 FDA UDI
Basic UDI-DI
880972899873H EUDAMED
510(k) Number
K231967 FDA UDI
FDA Product Code
NHA FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Angled Abutment by Megagen Implant Co. Ltd — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (3)

  • FDA UDI cf49c739-26c2-4fdd-8018-11b5d5afaeaa 35 fields · synced Oct 8, 2026
  • FDA UDI 51d0e104-329b-487f-91b8-3e9040a076b9 35 fields · synced May 30, 2026
  • EUDAMED f970686a-1d7e-454a-9b98-81ac349d9db3 61 fields · synced Oct 7, 2026