510(k) Report

510(k) · Cleared

Cleared

Jiangsu Healthy Way Mechanicl Wheelchair

K112950510(k) TraditionalCleared Mar 28, 2012176-day reviewClass I21 CFR 890.3850

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Jiangsu Healthy Medical Equipment Co;Ltd · IOR Wheelchair, Mechanical

Cleared on Mar 28, 2012 as substantially equivalent to K101999 (Guangdong Kaiyang Medical Technology Co., Ltd., 2010) after a 176-day review. Its family tree reaches back 7 generations to 2002.

Decided
Mar 28, 2012
Review
176 days
Class
Class I
Product code
IOR
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K020472 (2002). No later device cites it as a predicate yet.

  1. Root · 7 generations backK020472 Biotech Manual Wheelchair B900 Super Light WheelchairTaiwan Armada Enterprise Co., Ltd. · 2002
  2. 6 generations backK041337 Pro Walker ML-300 Foldable WheelchairPro Walker, Inc. · 2004
  3. 5 generations backK050290 Lerado, CoscoLerado Oversea Ltd. Twn Branch (Bvi) · 2005
  4. 4 generations backK050708 Lerado, Avanticare Mechanical Wheelchair, MR-9000Lerado Oversea Ltd. Twn Branch (Bvi) · 2005
  5. 3 generations backK051482 Jan Mao Wheelchair, Model JMC612-F18EPPJan Mao Industries Co., Ltd. · 2005
  6. 2 generations backK062218 Jan Mao Wheelchair, Models JMC612-FL318EPP and JMC612-FL418EPPJan Mao Industries Co., Ltd. · 2006
  7. 1 generation backK101999 Kaiyang Steel WheelchairGuangdong Kaiyang Medical Technology Co., Ltd. · 2010
  8. This deviceK112950 Jiangsu Healthy Way Mechanicl WheelchairJiangsu Healthy Medical Equipment Co;Ltd · 2012
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K020472Biotech Manual Wheelchair B900 Super Light WheelchairTaiwan Armada Enterprise Co., Ltd.2002—
−6K041337Pro Walker ML-300 Foldable WheelchairPro Walker, Inc.2004—
−5K050290Lerado, CoscoLerado Oversea Ltd. Twn Branch (Bvi)2005—
−4K050708Lerado, Avanticare Mechanical Wheelchair, MR-9000Lerado Oversea Ltd. Twn Branch (Bvi)2005—
−3K051482Jan Mao Wheelchair, Model JMC612-F18EPPJan Mao Industries Co., Ltd.2005—
−2K062218Jan Mao Wheelchair, Models JMC612-FL318EPP and JMC612-FL418EPPJan Mao Industries Co., Ltd.2006—
−1K101999Kaiyang Steel WheelchairGuangdong Kaiyang Medical Technology Co., Ltd.2010—
0 (this device)K112950Jiangsu Healthy Way Mechanicl WheelchairJiangsu Healthy Medical Equipment Co;Ltd2012—
FIG. 1 — Lineage of K112950, 2002–2012Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in IOR? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new IOR device

  1. #1 K201461 Manual Wheelchair, Model A011score 20.0 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K101999Kaiyang Steel Wheelchair
Summary page 2
…0 IS07176-22 Wheelchairs - Part 2 2:Set-up procedures, 2000. Legally marketed device for substantial equivalence comparison: . KAJYANG Steel Wheelchair (K 10 1999) Summary for substantial equivalence comparison: From the above comparison table the intended use between the subject d…
Guangdong Kaiyang Medical Technology Co., Ltd.2010—

Also cleared against K101999: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 10 years and passes through 6 companies; a new generation was cleared every 1.1 years on median.
  • None of the 7 ancestors has a recall.
  • 1 other device also cites its predicate K101999.

How does its category compare?

All IOR devices

IOR Wheelchair, Mechanical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · IOR

17so far in 2026, the most since 2007

2007: 52008: 132009: 42010: 122011: 62012: 112013: 72014: 72015: 32016: 102017: 72018: 32019: 62020: 22021: 22022: 42023: 92024: 42025: 72026 (partial year): 17
2007high 17 (2026) · low 2 (2020)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IOR

91in 2025

2007: 38 days median2008: 32 days median2009: 43 days median2010: 81 days median2011: 58 days median2012: 176 days median2013: 233 days median2014: 211 days median2015: 104 days median2016: 135 days median2017: 209 days median2018: 203 days median2019: 160 days median2022: 150 days median2023: 61 days median2024: 65 days median2025: 91 days median2026 (partial year): 103 days median
2007high 233 (2013) · low 32 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · IOR

1in 2021

2007: 12008: 32009: 22011: 62012: 32013: 32014: 32016: 12021: 1
2007high 6 (2011) · low 0 (2010)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · IOR

135in 2025

2007: 362008: 622009: 542010: 692011: 2322012: 1,2382013: 4,6742014: 5,0822015: 4,4722016: 1,8602017: 492018: 582019: 532020: 432021: 592022: 372023: 1652024: 1382025: 135
2007high 5,082 (2014) · low 36 (2007)2025

MAUDE reports naming product code IOR, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007538136
20081332362
2009443254
20101281069
20116586232
20121117631,238
2013723334,674
2014721135,082
2015310404,472
20161013511,860
20177209049
20183203058
20196160053
20202—043
20212—159
20224150037
20239610165
20244650138
20257910135
2026171030—

What is it indicated for?

The device is intended for medical purposes to provide mobility to persons restricted to a sitting position.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K112950: Jiangsu Healthy Way Mechanicl Wheelchair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K112950

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026