Manual Wheelchair (LW01108)— 510(k) K260642

Name: FDA 510(k) clearance K260642
Creator: U.S. Food and Drug Administration
Published: 2026-06-02

Substantially Equivalent

Anhui Longway Medical Technology Co., Ltd.

FDA 510(k) clearance K260642 for Manual Wheelchair (LW01108), Substantially Equivalent on 2026-06-02. Applicant: Anhui Longway Medical Technology Co., Ltd.. Device class: 1.

Clearance details

Applicant: Anhui Longway Medical Technology Co., Ltd.
Product code: Code IOR
Device class: Class 1
Regulation: 21 CFR 890.3850
Advisory panel: Physical Medicine
Date received: 2026-02-27
Decision date: 2026-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mingguang, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code IOR

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K261571 — Manual Wheelchair (H008, PCK7)2026-08-06
K252370 — GEN 4 JOY Wheelchair2026-07-24
K261075 — Manual Wheelchair (MS01); Manual Wheelchair (MA01)2026-06-22
K261076 — Caregiver-assisted wheelchair (MS02); Caregiver-assisted wheelchair (MA02)2026-06-22
K260849 — ICON 35; ICON 45; ICON 60; ICON 30FAF2026-06-11

More clearances from Anhui Longway Medical Technology Co., Ltd.

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K250366 — Electric Wheelchair (LW01301A07)2025-04-08

Adverse events under product code IOR

product code IOR

Death: 10
Injury: 232
Other: 2
Total: 244

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.