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Rhino Knee Immobilizer - 14 inch

by MD Orthopaedics

Rhino Knee Immobilizer - 14 inch (27183) is a Class I device made by MD Orthopaedics, listed in FDA GUDID since 20 Dec 2023 (UDI-DI 00810060887622), 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 Number00810060887622 UDI-DI Date20 Dec 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  • Withdrawn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
Rhino
Generic name
Knee splint
Model / Ref / Catalog
Knee Immobilizer - 14 inch, 27183
Primary DI / UDI-DI
00810060887622
FDA product code
ITQ
GMDN term
Knee splint
Device class
Class I
Regulation number
890.3475
GUDID distribution status
In Commercial Distribution

Related devices

Category: Knee immobilizer

Similar devices

Also classified as Knee immobilizer.

Other devices from MD Orthopaedics

See all devices from MD Orthopaedics →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)