510(k) Report

510(k) · Cleared

Cleared

Electric Scooter (DDF100)

K252275510(k) TraditionalCleared Jan 29, 2026191-day reviewClass II21 CFR 890.3800

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

Zhejiang Nysin Medical Co., Ltd. · INI Vehicle, Motorized 3-Wheeled

Cleared on Jan 29, 2026 as substantially equivalent to K201196 (Nanjing Jin Bai HE Medical Apparatus Co., Ltd., 2021) and 1 other predicate after a 191-day review. Its family tree reaches back 9 generations to 1992.

Decided
Jan 29, 2026
Review
191 days
Class
Class II
Product code
INI
Recalls
None
Predicates
2

Its longest line of descent runs back 9 generations to K923193 (1992). 12 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 9 generations backK923193 Sunrunner TE-777Pride Health Care, Inc. · 1992
  2. 5 generations between
  3. 3 generations backK182471 ScooterTianjin Kepler Vehicle Industry Co., Ltd. · 2019
  4. 2 generations backK201196 Scooter (Model: FDB01)Nanjing Jin Bai HE Medical Apparatus Co., Ltd. · 2021
  5. 1 generation backK242982 Mobility Scooter (MS160A)Suzhou Master Machinery Manufacturing Co.,Ltd · 2025
  6. This deviceK252275 Electric Scooter (DDF100)Zhejiang Nysin Medical Co., Ltd. · 2026
Show all 9 generations
  1. Root · 9 generations backK923193 Sunrunner TE-777Pride Health Care, Inc. · 1992
  2. 8 generations backK012791 C.T.M. Mobility Scooter Model # HS-320Warepalmy Enterprise, LLC (Usa) · 2001
  3. 7 generations backK031272 C.T.M. Mobility Scooter, Model HS-120C.T.M. Homecare Product, Inc. · 2003
  4. 6 generations backK032919 C.T.M. Mobility Scooter, Model HS-250C.T.M. Homecare Product, Inc. · 2003
  5. 5 generations backK070603 C.T.M. Mobilitty Scooter # HS-295C.T.M. Homecare Product, Inc. · 2007
  6. 4 generations backK162952 C.T.M. Mobility ScooterChien TI Enterprise Co., Ltd. · 2017
  7. 3 generations backK182471 ScooterTianjin Kepler Vehicle Industry Co., Ltd. · 2019
  8. 2 generations backK201196 Scooter (Model: FDB01)Nanjing Jin Bai HE Medical Apparatus Co., Ltd. · 2021
  9. 1 generation backK242982 Mobility Scooter (MS160A)Suzhou Master Machinery Manufacturing Co.,Ltd · 2025
  10. This deviceK252275 Electric Scooter (DDF100)Zhejiang Nysin Medical Co., Ltd. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K923193Sunrunner TE-777Pride Health Care, Inc.1992—
−8K012791C.T.M. Mobility Scooter Model # HS-320Warepalmy Enterprise, LLC (Usa)2001—
−7K031272C.T.M. Mobility Scooter, Model HS-120C.T.M. Homecare Product, Inc.2003—
−6K032919C.T.M. Mobility Scooter, Model HS-250C.T.M. Homecare Product, Inc.2003—
−5K070603C.T.M. Mobilitty Scooter # HS-295C.T.M. Homecare Product, Inc.2007—
−4K162952C.T.M. Mobility ScooterChien TI Enterprise Co., Ltd.2017—
−3K182471ScooterTianjin Kepler Vehicle Industry Co., Ltd.2019—
−2K201196Scooter (Model: FDB01)Nanjing Jin Bai HE Medical Apparatus Co., Ltd.2021—
−1K242982Mobility Scooter (MS160A)Suzhou Master Machinery Manufacturing Co.,Ltd2025—
0 (this device)K252275Electric Scooter (DDF100)Zhejiang Nysin Medical Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201110
201210
201810
FIG. 1 — Lineage of K252275, 1992–2026Source: 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 INI? 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 INI device

  1. #1 K231428 Mobility Scooter (Models: W3431D)score 23.1 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

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
*K201196Scooter (Model: FDB01)
Summary page 5
…21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K201196 Scooter (Model: FDBO1) I FNI K242982…
Nanjing Jin Bai HE Medical Apparatus Co., Ltd.2021—
*K242982Mobility Scooter (MS160A)
Summary page 5
…t) Product Code K201196 Scooter (Model: FDBO1) I FNI K242982 Mobility Scooter (MS160A) I FNI Device Description Su…
Suzhou Master Machinery Manufacturing Co.,Ltd2025—

Also cleared against K201196: 5 other devices →

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 34 years and passes through 8 companies; a new generation was cleared every 2.2 years on median.
  • None of the 12 ancestors has a recall.
  • 5 other devices also cite its predicate K201196.

How does its category compare?

All INI devices

INI Vehicle, Motorized 3-Wheeled: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · INI

21so far in 2026, the most since 2007

2007: 182008: 72009: 122010: 52011: 52012: 12013: 22014: 12015: 92016: 12017: 52018: 32019: 42020: 12021: 52022: 62023: 92024: 82025: 152026 (partial year): 21
2007high 21 (2026) · low 1 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · INI

111in 2025

2007: 29 days median2008: 28 days median2009: 41 days median2010: 46 days median2011: 130 days median2015: 202 days median2017: 191 days median2018: 266 days median2019: 298 days median2021: 575 days median2022: 159 days median2023: 123 days median2024: 137 days median2025: 111 days median2026 (partial year): 108 days median
2007high 575 (2021) · low 28 (2008)2026

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

Recalls per year · INI

1in 2013

2007: 22010: 32011: 32013: 1
2007high 3 (2010) · low 0 (2008)2026

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

Adverse event reports per year · INI

26in 2025

2007: 642008: 292009: 252010: 562011: 702012: 1722013: 4542014: 5672015: 1512016: 762017: 452018: 512019: 252020: 262021: 412022: 412023: 322024: 312025: 26
2007high 567 (2014) · low 25 (2009)2025

MAUDE reports naming product code INI, 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
20071829264
2008728029
20091241025
2010546356
20115130370
20121—0172
20132—1454
20141—0567
201592020151
20161—076
20175191045
20183266051
20194298025
20201—026
20215575041
20226159041
20239123032
20248137031
202515111026
2026211080—

What is it indicated for?

The electric scooter is a motor driven, indoor and outdoor transportation vehicle with the intended use to provide mobility to a disabled or elderly person limited to a seated position.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K252275: Electric Scooter (DDF100).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K252275

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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