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Smart Correction 50-1012-21A-WB

by Wishbone Medical Inc.

Smart Correction 50-1012-21A-WB is a Class II device made by Wishbone Medical Inc., listed in FDA GUDID since 2 Feb 2023 (UDI-DI B56250101221AWB0), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 NumberB56250101221AWB0 UDI-DI Date2 Feb 2023ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Smart Correction
Generic name
External orthopaedic fixation system, single-use
Model / Ref / Catalog
50-1012-21A-WB
Primary DI / UDI-DI
B56250101221AWB0
FDA product code
KTT
GMDN term
External orthopaedic fixation system, single-use
Device class
Class II
Regulation number
888.3030
GUDID distribution status
Not in Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Wishbone Medical Inc.

See all devices from Wishbone Medical Inc. →

Properties

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