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Henry Schein 1010827

by Henry Schein, Inc.

Henry Schein 1010827 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 15 May 2019 (UDI-DI 10304040038939), 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 Number10304040038939 UDI-DI Date15 May 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Henry Schein
Generic name
Denture cleanser
Model / Ref / Catalog
1010827
Primary DI / UDI-DI
10304040038939
FDA product code
FLG
GMDN term
Denture cleanser
Device class
Class I
Regulation number
880.6150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Denture cleanser

Similar devices

Other devices filed under FDA product code FLG (Cleaner, ultrasonic, medical instrument).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)