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FO Micro Screw System BTSC00024

by Field Orthopaedics Pty Ltd

FO Micro Screw System BTSC00024 is a Class I device made by Field Orthopaedics Pty Ltd, listed in FDA GUDID since 19 May 2020 (UDI-DI 09353903002475), 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 Number09353903002475 UDI-DI Date19 May 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  • Withdrawn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
FO Micro Screw System
Generic name
Surgical depth gauge, reusable
Model / Ref / Catalog
BTSC00024
Primary DI / UDI-DI
09353903002475
FDA product code
HTJ
GMDN term
Surgical depth gauge, reusable
Device class
Class I
Regulation number
888.4300
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)