Skip to content

Nupro® 130211

by Dentsply Professional

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD0031302111 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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 cavity varnish
Model / reference
130211
Primary DI / UDI-DI
D0031302111
FDA product code
LBH
GMDN term
Dental cavity varnish
Device class
Class II
Regulation number
872.3260
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental cavity varnish

Other devices from Dentsply Professional

See all devices from Dentsply Professional →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Manufacturing date: No