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Articulating Leg Rests 10273

by Dynarex Corp.

Articulating Leg Rests 10273 is a Class I device made by Dynarex Corp., listed in FDA GUDID since 6 Sep 2022 (UDI-DI 00840117324121), 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 Number00840117324121 UDI-DI Date6 Sep 2022ListedStatusListed 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  • Withdrawn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
Articulating Leg Rests
Generic name
Wheelchair footrest/legrest
Model / reference
10273
Primary DI / UDI-DI
00840117324121
FDA product code
KNO
GMDN term
Wheelchair footrest/legrest
Device class
Class I
Regulation number
890.3910
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KNO (Accessories, Wheelchair).

Other devices from Dynarex Corp.

See all devices from Dynarex Corp. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)