510(k) · Cleared
ClearedVimove
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dorsa VI Pty., Ltd. · IKN Electromyograph, Diagnostic
Cleared on Jul 11, 2014 as substantially equivalent to K063447 (Fasstech, 2007) and 1 other predicate after a 449-day review. Its family tree reaches back 4 generations to 1998.
- Decided
- Jul 11, 2014
- Review
- 449 days
- Class
- Class II
- Product code
- IKN
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 4 generations to K971407 (1998). 7 ancestors in all, the oldest K811172 (1981). No later device cites it as a predicate yet.
- Root · 4 generations backK971407 Jtech Commander and AlgometerJ-Tech Medical, Inc. · 1998
- 3 generations backK011964 Insight Millennium PlusFasstech · 2001
- 2 generations backK023209 Insight Millennium IiiFasstech · 2003
- 1 generation backK063447 Insight DiscoveryFasstech · 2007
- This deviceK131094 VimoveDorsa VI Pty., Ltd. · 2014
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K971407 | Jtech Commander and Algometer | J-Tech Medical, Inc. | 1998 | — |
| −3 | K011964 | Insight Millennium Plus | Fasstech | 2001 | — |
| −2 | K023209 | Insight Millennium Iii | Fasstech | 2003 | — |
| −1 | K063447 | Insight Discovery | Fasstech | 2007 | — |
| 0 (this device) | K131094 | Vimove | Dorsa VI Pty., Ltd. | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1981 | 1 | 0 |
| 1993 | 1 | 0 |
| 1999 | 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 IKN? 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K063447 | Insight DiscoverySummary page 2…Vicon _________________________________ ________ Discovery 510(k) Number K131094 K063447 K811172 Manufacturer dorsaVi Fasstech Oxford… | 2007 |
| * | K811172 | VICONSummary page 1…KQX (Goniometer). Predicate Devices: 1. Insight Discovery manufactured by Fasstech (K(063447). 2. Vicon manufactured by Oxford Medilog, Inc. (K8 11172). ViMove - Page 5-2… | 1981 |
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 16 years and passes through 3 companies; a new generation was cleared every 3.8 years on median.
- None of the 7 ancestors has a recall.
How does its category compare?
All IKN devicesIKN Electromyograph, Diagnostic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · IKN
3in 2017
2026 to Oct 25, outlined.
Median 510(k) review, days · IKN
188in 2017
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IKN
1in 2010
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IKN
3in 2025
MAUDE reports naming product code IKN, 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 | 1 | — | 0 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 1 | — | 0 | 2 |
| 2010 | 0 | — | 1 | 1 |
| 2011 | 2 | — | 0 | 4 |
| 2012 | 1 | — | 0 | 4 |
| 2013 | 2 | — | 0 | 24 |
| 2014 | 1 | — | 0 | 3 |
| 2015 | 1 | — | 0 | 13 |
| 2016 | 0 | — | 0 | 11 |
| 2017 | 3 | 188 | 0 | 2 |
| 2018 | 0 | — | 0 | 5 |
| 2019 | 0 | — | 0 | 6 |
| 2020 | 0 | — | 0 | 1 |
| 2021 | 0 | — | 0 | 2 |
| 2022 | 0 | — | 0 | 2 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 1 |
| 2025 | 0 | — | 0 | 3 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
ViMove is a wireless medical device that measures, records, and reports movements and muscle activity of the lower back / lumbar spine. The system also measures range of motion in the sagittal and coronal anatomical planes.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K131094 · printed Nov 6, 2026
Cite this page
510(k) Report. “K131094: Vimove.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131094
Report an extraction error
Are you the manufacturer?
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