Home › Device types › KNO
Accessories, Wheelchair
FDA product code KNO · Class 1 · Physical Medicine
1,049
Registered devices
76
Adverse events
3
Recalls
35
510(k) clearances
Devices with this code
Spex — SPEX LIMITEDAxiom — KI MOBILITY, LLCPryor — PRYOR PRODUCTSHand Pad Palm Extenser — Otto Bock Mobility Solutions GmbHAxiom — KI MOBILITY, LLCSetmark Incorporated — SETMARK INC.Axiom — KI MOBILITY, LLCProbasics — Drive Devilbiss HealthcareAxiom — KI MOBILITY, LLCTWISTER — Pride Mobility Products CorpSpex — SPEX LIMITEDAxiom — KI MOBILITY, LLCAxiom — KI MOBILITY, LLCAxiom — KI MOBILITY, LLCVive — VIVE HEALTH LLCAxiom — KI MOBILITY, LLCTolt Technologies LLC — Tolt Technologies LLCSpex — SPEX LIMITEDDRIVE — Drive Devilbiss HealthcareAxiom — KI MOBILITY, LLCAxiom — KI MOBILITY, LLCBD — PRYOR PRODUCTSVIVE — VIVE HEALTH LLCAxiom — KI MOBILITY, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-03-02 | Merits Holdings Co. dba Merits Health Products, Inc. | Pinion gear may disengage from track allowing lift to slip or jolt. |
| 2004-02-02 | Action Products Incorporated | Wheelchair seat may not properly support the user due to cracks in the plastic seat base. |
| 2002-05-14 | Action Products Incorporated | Wheelchair seat component is defective. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.