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Henry Schein Maxima 1126927

by Henry Schein, Inc.

Henry Schein Maxima 1126927 is a dental power tool converter attachment (FDA Class I; FDA product code EFB, Handpiece, air-powered, dental) made by Henry Schein, Inc., listed in FDA GUDID since 26 Aug 2020 (UDI-DI 00304040058138), 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 Number00304040058138 UDI-DI Date26 Aug 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  • Withdrawn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
Henry Schein Maxima
Generic name
Dental power tool converter attachment, rotary
Model / Ref / Catalog
1126927
Primary DI / UDI-DI
00304040058138
FDA product code
EFB
GMDN term
Dental power tool converter attachment, rotary
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental power tool converter attachment, rotary

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

  • Sterilise before use
  • Prescription use
  • Serial number
Other properties (12, all answered No)