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IH Angled Abutment

FDA UDI

Class II (US FDA UDI)

by sewon medix Inc.

Identity

Trade Name
IH Angled Abutment FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
SEWON MEDIX IH Angled Abutment Regular Hex_A-Type Non-Coating Set Product, Ø5.0x4.0mm 15° FDA UDI
Model / Reference
AIHAARA504015 FDA UDI
Description
SEWON MEDIX IH Angled Abutment Regular Hex_A-Type Non-Coating Set Product, Ø5.0x4.0mm 15° FDA UDI

Identifiers

Catalog Number
AIHAARA504015 FDA UDI
Primary DI / UDI-DI
08800041342327 FDA UDI
510(k) Number
K153521 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental implant suprastructure, permanent, preformed

IH Angled Abutment by sewon medix Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
sewon medix Inc.

Sources (1)

  • FDA UDI 0ed23b1e-4cec-444e-97ec-cb9c341ecf3c 36 fields · synced Jun 8, 2026