510(k) · Cleared
ClearedPeak Motus
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Peak Performance Technologies, Inc. · LXJ Interactive Rehabilitation Exercise Devices
Cleared on May 16, 2003 as substantially equivalent to K982425 (Pinsco Inc. Dba B & L Engineering, 1998) after a 71-day review. Its family tree reaches back 2 generations to 1989. 10 later devices descend from it.
- Decided
- May 16, 2003
- Review
- 71 days
- Class
- Class II
- Product code
- LXJ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K890076 (1989). 10 later devices descend from it, 4 citing it directly.
- Root · 2 generations backK890076 OrthotrakMotion Analysis Corp. · 1989
- 1 generation backK982425 Coda MPX30 Motion Analysis SystemPinsco Inc. Dba B & L Engineering · 1998
- This deviceK030714 Peak MotusPeak Performance Technologies, Inc. · 2003
- Descendant · cites it directly · 6 of its ownK130847 Jintronix Rehabilitation System (JRS)Jintronix, Inc. · 2014
- Descendant · 2 generations on · 1 of its ownK151446 Recovr Rehabilitation SystemRecovr,Inc · 2015
- Descendant · cites it directly · 1 of its ownK131660 Smart (Smart-D, Smart-DX)Bts S.P.A. · 2014
- Descendant · cites it directly · 0 of its ownK180880 DARI HealthScientific Analytics, Inc. · 2019
- Descendant · 2 generations on · 0 of its ownK171547 Qualisys Clinical SystemQualisys AB · 2018
Showing 5 of 10 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 10 · See all- K130847Jintronix Rehabilitation System (JRS)Jintronix, Inc. · 2014 · cites it directly6descendants
- K151446Recovr Rehabilitation SystemRecovr,Inc · 2015 · 2 generations on1descendant
- K131660Smart (Smart-D, Smart-DX)Bts S.P.A. · 2014 · cites it directly1descendant
- K180880DARI HealthScientific Analytics, Inc. · 2019 · cites it directly0descendants
- K171547Qualisys Clinical SystemQualisys AB · 2018 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K890076 | Orthotrak | Motion Analysis Corp. | 1989 | — |
| −1 | K982425 | Coda MPX30 Motion Analysis System | Pinsco Inc. Dba B & L Engineering | 1998 | — |
| 0 (this device) | K030714 | Peak Motus | Peak Performance Technologies, Inc. | 2003 | — |
| +1 | K130847 | Jintronix Rehabilitation System (JRS) | Jintronix, Inc. | 2014 | — |
| +2 | K151446 | Recovr Rehabilitation System | Recovr,Inc | 2015 | — |
| +1 | K131660 | Smart (Smart-D, Smart-DX) | Bts S.P.A. | 2014 | — |
| +1 | K180880 | DARI Health | Scientific Analytics, Inc. | 2019 | — |
| +2 | K171547 | Qualisys Clinical System | Qualisys AB | 2018 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 2 | 0 |
| 2015 | 3 | 0 |
| 2016 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 2 | 0 |
| 2019 | 1 | 0 |
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 LXJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K982425 | Coda MPX30 Motion Analysis SystemSummary page 1…System, Optical Position/Movement Recording Product code: LXJ Predicate Devices Trade Name: CODA mpx30 Motion Analysis System 51O(k) Number: K982425 Manufacturer: Charnwood Dynamics Ltd Introduction The Peak Motus Motion Measuring System is a mature product. It has been… | 1998 |
What descends from it? (10)
4 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 14 years and passes through 3 companies; a new generation was cleared every 9.7 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K130847 (Jintronix, Inc., 2014) has gone furthest, with 6 descendants of its own.
- 1 other device also cites its predicate K982425.
How does its category compare?
All LXJ devicesLXJ Interactive Rehabilitation Exercise Devices: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LXJ
3in 2019
2026 to Oct 25, outlined.
Median 510(k) review, days · LXJ
224in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LXJ
No recall names LXJ since 2007.
Adverse event reports per year · LXJ
1in 2018
MAUDE reports naming product code LXJ, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 2 | — | 0 | 0 |
| 2015 | 3 | 182 | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 2 | — | 0 | 0 |
| 2018 | 3 | 231 | 0 | 1 |
| 2019 | 3 | 224 | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
Computer and video system used to quantify and graphically display human movement patterns and techniques for uses such as assessment and training of limb or body motion in gait analysis, prosthetic design, pre/post rehabilitation evaluation, physical therapy, and the like.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K030714 · printed Nov 5, 2026
Cite this page
510(k) Report. “K030714: Peak Motus.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K030714
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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