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Multi-unit Abutment

FDA UDI

Class I (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name
Multi-unit Abutment FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, reusable FDA UDI
Device Name
Lab Screw Multi-unit Angled CC RP/WP and Ext Hex RP FDA UDI
Model / Reference
37897 FDA UDI
Description
Lab Screw Multi-unit Angled CC RP/WP and Ext Hex RP FDA UDI

Identifiers

Catalog Number
37897 FDA UDI
Primary DI / UDI-DI
07332747087505 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental implant suprastructure, temporary, preformed, reusable

Multi-unit Abutment by Nobel Biocare AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nobel Biocare AG

Sources (1)

  • FDA UDI 6b53fe32-806a-4607-b2d5-b08f4b195043 35 fields · synced May 30, 2026