Skip to content

Nupro® 965750

by Dentsply Professional

Nupro® 965750 is a Class I device made by Dentsply Professional, listed in FDA GUDID since 24 Nov 2022 (UDI-DI D0039657501), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD0039657501 UDI-DI Date24 Nov 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Nupro®
Generic name
Dental polishing cup, single-use
Model / Ref / Catalog
965750
Primary DI / UDI-DI
D0039657501
FDA product code
EGS
GMDN term
Dental polishing cup, single-use
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution

Other devices from Dentsply Professional

See all devices from Dentsply Professional →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)