510(k) Report

510(k) · Cleared

Cleared

Baide

K150009510(k) TraditionalCleared Feb 25, 201554-day reviewClass II21 CFR 888.3030

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

Jiangsu Baide Medical Intrument Co., Ltd. · HRS Plate, Fixation, Bone

Cleared on Feb 25, 2015 as substantially equivalent to K133840 (Suzhou Kangli Orthopaedics Instrument Co., Ltd., 2014) and 1 other predicate after a 54-day review. Its family tree reaches back 9 generations to 1998. 1 later device descends from it.

Decided
Feb 25, 2015
Review
54 days
Class
Class II
Product code
HRS
Recalls
None
Predicates
2

Its longest line of descent runs back 9 generations to K981372 (1998). 18 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 9 generations backK981372 Synthes 3.0 MM PC-Fix SystemSynthes (Usa) · 1998
  2. 5 generations between
  3. 3 generations backK100721 Locking Bone Screw Model HCQ04, HCZ04Changzhou Orthmar Medical Instrument Co., Ltd. · 2010
  4. 2 generations backK130340 Locking Bone Plates and ScrewsWeigao Orthopaedic Device Co., Ltd. · 2013
  5. 1 generation backK133840 Kangli Locking Plate SystemSuzhou Kangli Orthopaedics Instrument Co., Ltd. · 2014
  6. This deviceK150009 BaideJiangsu Baide Medical Intrument Co., Ltd. · 2015
  7. Descendant · cites it directly · 0 of its ownK240958 Locking Plates and Screws SystemsHebei Ruihe Medical Devices Co., Ltd. · 2025
Show all 9 generations
  1. Root · 9 generations backK981372 Synthes 3.0 MM PC-Fix SystemSynthes (Usa) · 1998
  2. 8 generations backK991407 Synthes Locking Calcaneal PlatesSynthes (Usa) · 1999
  3. 7 generations backK033669 Smith & Nephew Locking Bone Plate System (Locking Bone Plates and…Smith & Nephew, Inc. · 2003 · Recalled
  4. 6 generations backK050457 Merete Metafix Small Fragment Bone Plate SystemMerete Medical GmbH · 2005
  5. 5 generations backK063487 Merete BLP Small Fragment Locking Bone PlateMerete Medical GmbH · 2007
  6. 4 generations backK081513 Merete 3.0 and 3.5 MM Locking ScrewsMerete Medical GmbH · 2008
  7. 3 generations backK100721 Locking Bone Screw Model HCQ04, HCZ04Changzhou Orthmar Medical Instrument Co., Ltd. · 2010
  8. 2 generations backK130340 Locking Bone Plates and ScrewsWeigao Orthopaedic Device Co., Ltd. · 2013
  9. 1 generation backK133840 Kangli Locking Plate SystemSuzhou Kangli Orthopaedics Instrument Co., Ltd. · 2014
  10. This deviceK150009 BaideJiangsu Baide Medical Intrument Co., Ltd. · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K240958Locking Plates and Screws SystemsHebei Ruihe Medical Devices Co., Ltd. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K981372Synthes 3.0 MM PC-Fix SystemSynthes (Usa)1998—
−8K991407Synthes Locking Calcaneal PlatesSynthes (Usa)1999—
−7K033669Smith & Nephew Locking Bone Plate System (Locking Bone Plates and Screws)Smith & Nephew, Inc.20031
−6K050457Merete Metafix Small Fragment Bone Plate SystemMerete Medical GmbH2005—
−5K063487Merete BLP Small Fragment Locking Bone PlateMerete Medical GmbH2007—
−4K081513Merete 3.0 and 3.5 MM Locking ScrewsMerete Medical GmbH2008—
−3K100721Locking Bone Screw Model HCQ04, HCZ04Changzhou Orthmar Medical Instrument Co., Ltd.2010—
−2K130340Locking Bone Plates and ScrewsWeigao Orthopaedic Device Co., Ltd.2013—
−1K133840Kangli Locking Plate SystemSuzhou Kangli Orthopaedics Instrument Co., Ltd.2014—
0 (this device)K150009BaideJiangsu Baide Medical Intrument Co., Ltd.2015—
+1K240958Locking Plates and Screws SystemsHebei Ruihe Medical Devices Co., Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
199910
200030
200110
200210
200610
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K150009, 1998–2025Source: 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 HRS? 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 HRS device

  1. #1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 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
*K133840Kangli Locking Plate System
Summary page 5
…K150009 page 2 of 3 P a g e |2 510 (k) Number: K133840 Product Name: Locking Bone Plates and Scews Submitter: Suzhou Kangli Orthopaedic Instrument Co., Ltd. Predicate Devices #2: 510…
Suzhou Kangli Orthopaedics Instrument Co., Ltd.2014—
*K130340Locking Bone Plates and Screws
Summary page 5
…2 510 (k) Number: K133840 Product Name: Locking Bone Plates and Scews Submitter: Suzhou Kangli Orthopaedic Instrument Co., Ltd. Predicate Devices #2: 510 (k) Number: K130340 Product Name: Locking Bone Plates and Scews Submitter: Weigao Orthopaedic Device Co., Ltd. 5. Device Description BaiDe® locking…
Weigao Orthopaedic Device Co., Ltd.2013—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K240958Locking Plates and Screws SystemsHebei Ruihe Medical Devices Co., Ltd.20250

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 17 years and passes through 7 companies; a new generation was cleared every 1.5 years on median.
  • 4 of the 18 ancestors have a recall of any class.
  • Of its descendants, K240958 (Hebei Ruihe Medical Devices Co., Ltd., 2025) has gone furthest, with 0 descendants of its own.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · HRS

54in 2025

2007: 352008: 352009: 472010: 492011: 432012: 592013: 562014: 762015: 562016: 442017: 572018: 402019: 462020: 482021: 402022: 472023: 402024: 542025: 542026 (partial year): 51
2007high 76 (2014) · low 35 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HRS

90in 2025

2007: 63 days median2008: 87 days median2009: 85 days median2010: 100 days median2011: 88 days median2012: 106 days median2013: 89 days median2014: 57 days median2015: 97 days median2016: 109 days median2017: 122 days median2018: 116 days median2019: 89 days median2020: 88 days median2021: 87 days median2022: 144 days median2023: 120 days median2024: 96 days median2025: 90 days median2026 (partial year): 82 days median
2007high 144 (2022) · low 57 (2014)2026

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

Recalls per year · HRS

1in 2025

2007: 22008: 112009: 32010: 162011: 52012: 42013: 112015: 72016: 52017: 32018: 22019: 252020: 12021: 92022: 32023: 12025: 12026 (partial year): 3
2007high 25 (2019) · low 0 (2014)2026

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

Adverse event reports per year · HRS

2,306in 2025

2007: 3392008: 3112009: 4352010: 4912011: 7732012: 1,6632013: 2,6432014: 2,4132015: 3,0952016: 2,2762017: 2,2202018: 2,6632019: 3,3592020: 2,7902021: 2,4422022: 1,7002023: 2,0492024: 1,8492025: 2,306
2007high 3,359 (2019) · low 311 (2008)2025

MAUDE reports naming product code HRS, 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
200735632339
2008358711311
200947853435
20104910016491
201143885773
20125910641,663
20135689112,643
2014765702,413
2015569773,095
20164410952,276
20175712232,220
20184011622,663
20194689253,359
2020488812,790
2021408792,442
20224714431,700
20234012012,049
2024549601,849
2025549012,306
202651823—

What is it indicated for?

BaiDe® locking plate system is intended for adult patients as indicated for fixation of fractures of tibia.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K150009: Baide.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K150009

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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