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Henry Schein 5703802

by Henry Schein, Inc.

Henry Schein 5703802 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 8 Aug 2024 (UDI-DI 10304040185275), 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 Number10304040185275 UDI-DI Date8 Aug 2024ListedStatusListed 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  • Withdrawn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
Ultrasonic-cleaning water bath
Model / Ref / Catalog
5703802
Primary DI / UDI-DI
10304040185275
FDA product code
FLG
GMDN term
Ultrasonic-cleaning water bath
Device class
Class I
Regulation number
880.6150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ultrasonic-cleaning water bath

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

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)