Skip to content

Henry Schein 5702771

by Henry Schein, Inc.

Henry Schein 5702771 is a Class II device made by Henry Schein, Inc., listed in FDA GUDID since 15 Jan 2025 (UDI-DI 00304040155837), 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 Number00304040155837 UDI-DI Date15 Jan 2025ListedStatusListed 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  • Withdrawn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 dental scaling/debridement system
Model / Ref / Catalog
5702771
Primary DI / UDI-DI
00304040155837
FDA product code
ELC
GMDN term
Ultrasonic dental scaling/debridement system
Device class
Class II
Regulation number
872.4850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ultrasonic dental scaling/debridement system

Similar devices in this category

Other devices filed under Ultrasonic dental scaling/debridement system.

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)