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SurgiPro 5701731

by Henry Schein, Inc.

SurgiPro 5701731 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 31 Jan 2020 (UDI-DI 00304040125687), 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 Number00304040125687 UDI-DI Date31 Jan 2020ListedStatusListed 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  • Withdrawn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
SurgiPro
Generic name
Dental power tool system handpiece, pneumatic
Model / Ref / Catalog
5701731
Primary DI / UDI-DI
00304040125687
FDA product code
EFB
GMDN term
Dental power tool system handpiece, pneumatic
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental power tool system handpiece, pneumatic

Similar devices

Other devices filed under FDA product code EFB (Handpiece, air-powered, dental).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Serial number
Other properties (14, all answered No)