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Splint, Universal Buck's Traction 1300

by Mizuho Orthopedic Systems, Inc.

Splint, Universal Buck's Traction 1300 is a Class I device made by Mizuho Orthopedic Systems, Inc., listed in FDA GUDID since 27 Jul 2020 (UDI-DI 00842430112270), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842430112270 UDI-DI Date27 Jul 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  • Withdrawn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
Splint, Universal Buck's Traction
Generic name
Traction boot
Model / Ref / Catalog
1300
Primary DI / UDI-DI
00842430112270
FDA product code
HSP
GMDN term
Traction boot
Device class
Class I
Regulation number
888.5890
GUDID distribution status
In Commercial Distribution

Related devices

Category: Traction boot

Other devices from Mizuho Orthopedic Systems, Inc.

See all devices from Mizuho Orthopedic Systems, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)