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TopLock CD-TP-8030

by Fusion Orthopedics, LLC

TopLock CD-TP-8030 is a Class II device made by Fusion Orthopedics, LLC, listed in FDA GUDID since 21 Dec 2020 (UDI-DI 00840124501492), 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 Number00840124501492 UDI-DI Date21 Dec 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  • Withdrawn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
TopLock
Generic name
Cannulated surgical drill bit, single-use, non-sterile
Model / Ref / Catalog
CD-TP-8030
Description
Punch 3.0 mm Short
Primary DI / UDI-DI
00840124501492
FDA product code
MBI
GMDN term
Cannulated surgical drill bit, single-use, non-sterile
Device class
Class II
Regulation number
888.3040
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue).

Other devices from Fusion Orthopedics USA, LLC

  • FibFix FN-TH-4713-S

    Class II
  • FibFix FN-TH-4713

    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)