510(k) Report

510(k) · Cleared

Cleared

ARIX Wrist System

K151468510(k) TraditionalCleared Jan 14, 2016227-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

Jeil Medical Corporation · HRS Plate, Fixation, Bone

Cleared on Jan 14, 2016 as substantially equivalent to K103332 (Medartis AG, 2011) and 1 other predicate after a 227-day review. Its family tree reaches back 7 generations to 1996. 7 later devices descend from it.

Decided
Jan 14, 2016
Review
227 days
Class
Class II
Product code
HRS
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K962616 (1996). 21 ancestors in all, the oldest K885250 (1989). 7 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2007: 1 other ancestor2006: 1 other ancestor2004: 3 other ancestors2002: 1 other ancestor2000: 2 other ancestors1998: 1 other ancestor1996: 3 other ancestors1989: 1 other ancestor2017: 2 descendants cleared2019: 1 descendant cleared2018: 1 descendant cleared2020: 1 descendant cleared2023: 1 descendant cleared2024: 1 descendant clearedK962616 · Synthes Dorsal Distal Radius Plate (DDRP) System · Synthes (Usa) · 1996K982732 · Synthes (Usa) Distal Radius Plate System (DRPS) · Synthes · 1998×2: 2 generations cleared close together, K023007 (2002), K030198 (2003) K051567 · Aptus Titanium Osteosynthesis System · Medartis, Inc. · 2005 · recalledK103332 · Aptus Ulna Plates · Medartis AG · 2011K142906 · APTUS Wrist 2.5 System · Medartis AG · 20151990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 5 other ancestors3 generations back: 6 other ancestors4 generations back: 2 other ancestors5 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 3 descendants3 generations forward: 1 descendant K142906 · APTUS Wrist 2.5 System · Medartis AG · 2015K103332 · Aptus Ulna Plates · Medartis AG · 2011K051567 · Aptus Titanium Osteosynthesis System · Medartis, Inc. · 2005 · recalledK030198 · Hand Innovations, Inc. Distal Radius Fracture Repair System · Hand Innovations, Inc. · 2003K023007 · Distal Radius Fracture Repair System · Hand Innovations, Inc. · 2002K982732 · Synthes (Usa) Distal Radius Plate System (DRPS) · Synthes · 1998K962616 · Synthes Dorsal Distal Radius Plate (DDRP) System · Synthes (Usa) · 1996−50
  1. Root · 7 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
  2. 6 generations backK982732 Synthes (Usa) Distal Radius Plate System (DRPS)Synthes · 1998
  3. 5 generations backK023007 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2002
  4. 4 generations backK030198 Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  5. 3 generations backK051567 Aptus Titanium Osteosynthesis SystemMedartis, Inc. · 2005 · Recalled
  6. 2 generations backK103332 Aptus Ulna PlatesMedartis AG · 2011
  7. 1 generation backK142906 APTUS Wrist 2.5 SystemMedartis AG · 2015
  8. This deviceK151468 ARIX Wrist SystemJeil Medical Corporation · 2016
  9. Descendant · cites it directly · 3 of its ownK172008 ARIX Humerus SystemJeil Medical Corporation · 2017
  10. Descendant · cites it directly · 2 of its ownK170705 ARIX Wrist SystemJeil Medical Corporation · 2017
  11. Descendant · 2 generations on · 1 of its ownK202912 ARIX Ankle Distal Tibia SystemJeil Medical Corporation · 2020
  12. Descendant · 2 generations on · 1 of its ownK180972 ARIX Clavicle SystemJeil Medical Corporation · 2018
  13. Descendant · 3 generations on · 0 of its ownK232115 TDM Large Bone Plate and Screw SystemTdm Co., Ltd. · 2024

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2017: 22018: 12019: 12020: 12023: 12024: 1
2017high 2 (2017) · low 0 (2021)2026

Most influential descendants

Showing 5 of 7 · See all
  • K172008ARIX Humerus SystemJeil Medical Corporation · 2017 · cites it directly3descendants
  • K170705ARIX Wrist SystemJeil Medical Corporation · 2017 · cites it directly2descendants
  • K202912ARIX Ankle Distal Tibia SystemJeil Medical Corporation · 2020 · 2 generations on1descendant
  • K180972ARIX Clavicle SystemJeil Medical Corporation · 2018 · 2 generations on1descendant
  • K232115TDM Large Bone Plate and Screw SystemTdm Co., Ltd. · 2024 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K962616Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa)1996—
−6K982732Synthes (Usa) Distal Radius Plate System (DRPS)Synthes1998—
−5K023007Distal Radius Fracture Repair SystemHand Innovations, Inc.2002—
−4K030198Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−3K051567Aptus Titanium Osteosynthesis SystemMedartis, Inc.20051
−2K103332Aptus Ulna PlatesMedartis AG2011—
−1K142906APTUS Wrist 2.5 SystemMedartis AG2015—
0 (this device)K151468ARIX Wrist SystemJeil Medical Corporation2016—
+1K172008ARIX Humerus SystemJeil Medical Corporation2017—
+1K170705ARIX Wrist SystemJeil Medical Corporation2017—
+2K202912ARIX Ankle Distal Tibia SystemJeil Medical Corporation2020—
+2K180972ARIX Clavicle SystemJeil Medical Corporation2018—
+3K232115TDM Large Bone Plate and Screw SystemTdm Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199630
199810
200020
200210
200430
200610
200710
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201720
201810
201910
202010
202310
202410
FIG. 1 — Lineage of K151468, 1996–2024Source: 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
*K103332Aptus Ulna Plates
Summary page 5
…ation of Predicate Device(s) [21 CFR 807.92(a)(3)] The identified predicate devices within this submission are shown as follow; • 510(k) Number: K103332 • Applicant: Medartis AG • Common Name: plate, fixation, bone • Device Name:…
Medartis AG2011—
*K142906APTUS Wrist 2.5 System
Cleared while this submission was under review
Summary page 5
…Medartis AG • Common Name: plate, fixation, bone • Device Name: APTUS® Ulna Plates • 510(k) Number: K142906 • Applicant: Medartis • Common Name: Plate, fixation, bone…
Medartis AG2015—

Also cleared against K103332: 11 other devices →

What descends from it? (7)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K172008ARIX Humerus SystemJeil Medical Corporation20173
K170705ARIX Wrist SystemJeil Medical Corporation20172
K191972ARIX Wrist SystemJeil Medical Corporation20190

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 6 companies; a new generation was cleared every 2.4 years on median.
  • 5 of the 21 ancestors have a recall of any class.
  • Of its descendants, K172008 (Jeil Medical Corporation, 2017) has gone furthest, with 3 descendants of its own.
  • 11 other devices also cite its predicate K103332.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, 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?

The ARIX Wrist System(Radius) is intended for use in forearm fractures, osteotomies and arthrodesis. The ARIX Wrist System(Ulna) is intended for fractures and osteotomies, in particular for the ulna.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151468: ARIX Wrist System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151468

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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