510(k) Report

510(k) · Cleared

Cleared

Manual Wheelchair

K220671510(k) TraditionalCleared Jul 21, 2022136-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

Hebei Ruilangde Medical Equipment Technology Group Co., Ltd. · IOR Wheelchair, Mechanical

Cleared on Jul 21, 2022 as substantially equivalent to K180852 (Jiangyin Newrise Medical Equipment Co., Ltd., 2019) after a 136-day review. Its family tree reaches back 12 generations to 2002.

Decided
Jul 21, 2022
Review
136 days
Class
Class I
Product code
IOR
Recalls
None
Predicates
1

Its longest line of descent runs back 12 generations to K020472 (2002). No later device cites it as a predicate yet.

  1. Root · 12 generations backK020472 Biotech Manual Wheelchair B900 Super Light WheelchairTaiwan Armada Enterprise Co., Ltd. · 2002
  2. 8 generations between
  3. 3 generations backK153328 SUNCO Mechanical Wheelchair, model SKW-9003Danyang Sunco Machinery Co., Ltd. · 2016
  4. 2 generations backK163352 WheelchairKunshan Hi-Fortune Health Products Co., Ltd. · 2017
  5. 1 generation backK180852 Manual WheelchairJiangyin Newrise Medical Equipment Co., Ltd. · 2019
  6. This deviceK220671 Manual WheelchairHebei Ruilangde Medical Equipment Technology Group Co., Ltd. · 2022
Show all 12 generations
  1. Root · 12 generations backK020472 Biotech Manual Wheelchair B900 Super Light WheelchairTaiwan Armada Enterprise Co., Ltd. · 2002
  2. 11 generations backK041337 Pro Walker ML-300 Foldable WheelchairPro Walker, Inc. · 2004
  3. 10 generations backK050290 Lerado, CoscoLerado Oversea Ltd. Twn Branch (Bvi) · 2005
  4. 9 generations backK050708 Lerado, Avanticare Mechanical Wheelchair, MR-9000Lerado Oversea Ltd. Twn Branch (Bvi) · 2005
  5. 8 generations backK051482 Jan Mao Wheelchair, Model JMC612-F18EPPJan Mao Industries Co., Ltd. · 2005
  6. 7 generations backK062218 Jan Mao Wheelchair, Models JMC612-FL318EPP and JMC612-FL418EPPJan Mao Industries Co., Ltd. · 2006
  7. 6 generations backK101999 Kaiyang Steel WheelchairGuangdong Kaiyang Medical Technology Co., Ltd. · 2010
  8. 5 generations backK112816 Zhenjiang Asure Mechanical WheelchairZhenjiang Assure Medical Equipment Co., Ltd. · 2012
  9. 4 generations backK130017 Valentine Steel WheelchairValentine Intl., Ltd. · 2014
  10. 3 generations backK153328 SUNCO Mechanical Wheelchair, model SKW-9003Danyang Sunco Machinery Co., Ltd. · 2016
  11. 2 generations backK163352 WheelchairKunshan Hi-Fortune Health Products Co., Ltd. · 2017
  12. 1 generation backK180852 Manual WheelchairJiangyin Newrise Medical Equipment Co., Ltd. · 2019
  13. This deviceK220671 Manual WheelchairHebei Ruilangde Medical Equipment Technology Group Co., Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K020472Biotech Manual Wheelchair B900 Super Light WheelchairTaiwan Armada Enterprise Co., Ltd.2002—
−11K041337Pro Walker ML-300 Foldable WheelchairPro Walker, Inc.2004—
−10K050290Lerado, CoscoLerado Oversea Ltd. Twn Branch (Bvi)2005—
−9K050708Lerado, Avanticare Mechanical Wheelchair, MR-9000Lerado Oversea Ltd. Twn Branch (Bvi)2005—
−8K051482Jan Mao Wheelchair, Model JMC612-F18EPPJan Mao Industries Co., Ltd.2005—
−7K062218Jan Mao Wheelchair, Models JMC612-FL318EPP and JMC612-FL418EPPJan Mao Industries Co., Ltd.2006—
−6K101999Kaiyang Steel WheelchairGuangdong Kaiyang Medical Technology Co., Ltd.2010—
−5K112816Zhenjiang Asure Mechanical WheelchairZhenjiang Assure Medical Equipment Co., Ltd.2012—
−4K130017Valentine Steel WheelchairValentine Intl., Ltd.2014—
−3K153328SUNCO Mechanical Wheelchair, model SKW-9003Danyang Sunco Machinery Co., Ltd.2016—
−2K163352WheelchairKunshan Hi-Fortune Health Products Co., Ltd.2017—
−1K180852Manual WheelchairJiangyin Newrise Medical Equipment Co., Ltd.2019—
0 (this device)K220671Manual WheelchairHebei Ruilangde Medical Equipment Technology Group Co., Ltd.2022—
FIG. 1 — Lineage of K220671, 2002–2022Source: 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
*K180852Manual Wheelchair
Summary page 4
…ification Name: Wheelchair, Mechanical Classification: Class I Product code: IOR Regulation Number: 21 CFR 890.3850 Review Panel: Physical Medicine C. Predicate device: K180852 Manual Wheelchair JIANGYIN NEWRISE MEDICAL EQUIPMENT CO., LTD. D. Device Description: The Manual Wheelchair is a…
Jiangyin Newrise Medical Equipment Co., Ltd.2019—

Also cleared against K180852: 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 20 years and passes through 11 companies; a new generation was cleared every 1.6 years on median.
  • None of the 12 ancestors has a recall.
  • 1 other device also cites its predicate K180852.

How does its category compare?

All IOR devices

IOR Wheelchair, Mechanical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, 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 Manual Wheelchair 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. “K220671: Manual Wheelchair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K220671

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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