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Bone Mill Plus 5420100000

by Stryker Corp.

Bone Mill Plus 5420100000 (5420-100-000) is a Class I device made by Stryker Corp., listed in FDA GUDID since 22 Dec 2022 (UDI-DI 07613327542134), 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 Number07613327542134 UDI-DI Date22 Dec 2022ListedStatusListed 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  • Withdrawn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
Bone Mill Plus
Generic name
Powered bone mill motor
Model / Ref / Catalog
5420100000, 5420-100-000
Primary DI / UDI-DI
07613327542134
FDA product code
HWE
GMDN term
Powered bone mill motor
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Powered bone mill motor

Similar devices

Also classified as Powered bone mill motor.

Similar devices

Other devices filed under FDA product code HWE (INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT).

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)