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Nupro®

FDA UDI

Class I (US FDA UDI)

by Dentsply Professional

Identity

Trade Name
NUPRO® FDA UDI
Generic Name
Dental polishing cup, single-use FDA UDI
Device Name
NUPRO REVOLV SLIM DPA SOFT FDA UDI
Model / Reference
965067 FDA UDI
Description
NUPRO REVOLV SLIM DPA SOFT FDA UDI

Identifiers

Catalog Number
965067 FDA UDI
Primary DI / UDI-DI
D0039650671 FDA UDI
FDA Product Code
EGS FDA UDI
GMDN Term
Dental polishing cup, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental polishing cup, single-use

Nupro® by Dentsply Professional — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental polishing cup, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentsply Professional

Sources (1)

  • FDA UDI cdb7d90d-19dd-48ad-b84d-f8be8d9fdca3 34 fields · synced Jun 1, 2026