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EZ Slider 30051

by Therafin Corporation

EZ Slider 30051 is a Class I device made by Therafin Corporation, listed in FDA GUDID since 6 Jul 2023 (UDI-DI 00840252903090), 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 Number00840252903090 UDI-DI Date6 Jul 2023ListedStatusListed 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  • Withdrawn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
EZ Slider
Generic name
Assistive shoehorn/bootjack
Model / Ref / Catalog
30051
Primary DI / UDI-DI
00840252903090
FDA product code
ILD
GMDN term
Assistive shoehorn/bootjack
Device class
Class I
Regulation number
890.5050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Assistive shoehorn/bootjack

Other devices from Therafin Corporation

See all devices from Therafin Corporation →

Properties

  • Premarket exempt
  • Manufacturing date
Other properties (13, all answered No)