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FuzeRight FR-KW-416

by Fusion Orthopedics, LLC

FuzeRight FR-KW-416 is a Class II device made by Fusion Orthopedics, LLC, listed in FDA GUDID since 14 Apr 2021 (UDI-DI 00840124505117), 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 Number00840124505117 UDI-DI Date14 Apr 2021ListedStatusListed 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  • Withdrawn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
FuzeRight
Generic name
Orthopaedic bone wire
Model / Ref / Catalog
FR-KW-416
Primary DI / UDI-DI
00840124505117
FDA product code
HWC
GMDN term
Orthopaedic bone wire
Device class
Class II
Regulation number
888.3040
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic bone wire

Other devices from Fusion Orthopedics USA, LLC

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    Class II

  • FibFix FN-TH-5713

    Class II

  • FibFix FN-TH-5713-S

    Class II

See all devices from Fusion Orthopedics USA, LLC →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)