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i-Clean Angled Abutment

FDA UDI

Class I (US FDA UDI)

by Dentis Co. , Ltd

Identity

Trade Name
i-Clean Angled Abutment FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Dental Implant Abutment / i-Clean Angled Abutment / DIAA25S FDA UDI
Model / Reference
DIAA25S FDA UDI
Description
Dental Implant Abutment / i-Clean Angled Abutment / DIAA25S FDA UDI

Identifiers

Primary DI / UDI-DI
08806169166401 FDA UDI
510(k) Number
K082843 FDA UDI
FDA Product Code
HNA FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, permanent, preformed

i-Clean Angled Abutment by Dentis Co. , Ltd — Class I — 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
Dentis Co. , Ltd

Sources (1)

  • FDA UDI 893bbd5f-0ec7-47f6-95d6-5815c0585061 34 fields · synced Jun 1, 2026