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Vivid NuFill Unit Dose A3 D010484

by Pearson Dental Supplies, Inc.

Vivid NuFill Unit Dose A3 D010484 is a Class II device made by Pearson Dental Supplies, Inc., listed in FDA GUDID since 23 Jun 2016 (UDI-DI D724D0104840), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD724D0104840 UDI-DI Date23 Jun 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  • Withdrawn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
Vivid NuFill Unit Dose A3
Generic name
Light-cured dental restorative composite resin
Model / reference
D010484
Primary DI / UDI-DI
D724D0104840
FDA product code
EBF
GMDN term
Light-cured dental restorative composite resin
Device class
Class II
Regulation number
872.3690
GUDID distribution status
In Commercial Distribution

Related devices

Category: Light-cured dental restorative composite resin

Other devices from Pearson Dental Supplies, Inc.

See all devices from Pearson Dental Supplies, Inc. →

Properties

  • Single use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)