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Schick B1118051

by Dentsply International

Schick B1118051 is a Class II device made by Dentsply International, listed in FDA GUDID since 6 Nov 2024 (UDI-DI D003B11180510), 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 NumberD003B11180510 UDI-DI Date6 Nov 2024ListedStatusListed 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  • Withdrawn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
Schick
Generic name
Dental digital imaging sensor, intraoral
Model / Ref / Catalog
B1118051
Primary DI / UDI-DI
D003B11180510
FDA product code
EAP, MQB
GMDN term
Dental digital imaging sensor, intraoral
Device class
Class II
Regulation number
872.1810, 892.1680
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental digital imaging sensor, intraoral

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Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)