Identity

Trade Name
Nuvo FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
CEMENT RETAINED ABUTMENT IF FDA UDI
Model / Reference
CD1402001 FDA UDI
Description
CEMENT RETAINED ABUTMENT IF FDA UDI

Identifiers

Catalog Number
CD1402001 FDA UDI
Primary DI / UDI-DI
07899878038832 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3.5 Millimeter FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Nuvo by JJGC Indústria e Comércio de Materiais Dentários S/A. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 93295e31-3203-4393-b7f2-d051b8854476 37 fields · synced May 31, 2026