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FuzeFix Max FT CD-CS-1840-S

by Fusion Orthopedics, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840124524699 UDI-DI Date3 Nov 2025ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
FuzeFix Max FT
Generic Name
Cannulated surgical drill bit, single-use
Model / Ref / Catalog
CD-CS-1840-S
Primary DI / UDI-DI
00840124524699
510(k) Number
FDA Product Code
DZI
GMDN Term
Cannulated surgical drill bit, single-use
Device Class
Class II
Regulation Number
872.4120
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K170038)

Show all (12)

Other devices from Fusion Orthopedics USA, LLC

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No