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Cemented Abutment

FDA UDI

Class II (US FDA UDI)

by S.I.N. - Sistema DE Implante Nacional S.A.

Identity

Trade Name
Cemented Abutment FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
ABUTMENT CEMENTED MORSE Ø4,5 X4X6MM FDA UDI
Model / Reference
AIM 45604C FDA UDI
Description
ABUTMENT CEMENTED MORSE Ø4,5 X4X6MM FDA UDI

Identifiers

Catalog Number
AIM 45604C FDA UDI
Primary DI / UDI-DI
07899995216373 FDA UDI
510(k) Number
K170392 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Cemented Abutment by S.I.N. - Sistema DE Implante Nacional S.A. — 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

Sources (1)

  • FDA UDI b2e20130-1fc9-468c-9b88-4b44128e3076 35 fields · synced Jun 1, 2026