510(k) · Cleared
ClearedInbody
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Biospace Corporation Limited · MNW Analyzer, Body Composition
Cleared on Aug 19, 2011 as substantially equivalent to K052646 (Biospace Corporation Limited, 2005) and 1 other predicate after a 157-day review. Its family tree reaches back 6 generations to 1983. 3 later devices descend from it.
- Decided
- Aug 19, 2011
- Review
- 157 days
- Class
- Class II
- Product code
- MNW
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 6 generations to K830292 (1983). 14 ancestors in all. 3 later devices descend from it, 3 citing it directly.
- Root · 6 generations backK830292 Bioelectrical Impedance Analyzer #101Rjl Systems, Inc. · 1983
- 5 generations backK023478 Inbody AP1 Body Composition AnalyzerBiospace Co.,Ltd · 2003
- 4 generations backK042528 Inbody, Model 3.0Biospace Corporation Limited · 2005
- 3 generations backK052646 Biospace Body Composition Analyzers, Models Inbody 520, 720 and S20Biospace Corporation Limited · 2005
- 2 generations backK062603 Biospace Body Composition Analyzers, Model Inbody 230Biospace Corporation Limited · 2007
- 1 generation backK092786 Inbody, Models: 270, R20, R20BBiospace Corporation Limited · 2010
- This deviceK110689 InbodyBiospace Corporation Limited · 2011
- Descendant · cites it directly · 2 of its ownK123228 Inbody 770, Inbody 570, Inbody S10, Inbody H20/Inbody H20(B)Biospace Corporation Limited · 2013
- Descendant · cites it directly · 0 of its ownK141483 Biospace Body Composition AnalyzerBiospace Corporation Limited · 2014
- Descendant · cites it directly · 0 of its ownK130777 InbodyBiospace Corporation Limited · 2013
Most influential descendants
Showing 3 of 3 · See all- K123228Inbody 770, Inbody 570, Inbody S10, Inbody H20/Inbody H20(B)Biospace Corporation Limited · 2013 · cites it directly2descendants
- K141483Biospace Body Composition AnalyzerBiospace Corporation Limited · 2014 · cites it directly0descendants
- K130777InbodyBiospace Corporation Limited · 2013 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K830292 | Bioelectrical Impedance Analyzer #101 | Rjl Systems, Inc. | 1983 | — |
| −5 | K023478 | Inbody AP1 Body Composition Analyzer | Biospace Co.,Ltd | 2003 | — |
| −4 | K042528 | Inbody, Model 3.0 | Biospace Corporation Limited | 2005 | — |
| −3 | K052646 | Biospace Body Composition Analyzers, Models Inbody 520, 720 and S20 | Biospace Corporation Limited | 2005 | — |
| −2 | K062603 | Biospace Body Composition Analyzers, Model Inbody 230 | Biospace Corporation Limited | 2007 | — |
| −1 | K092786 | Inbody, Models: 270, R20, R20B | Biospace Corporation Limited | 2010 | — |
| 0 (this device) | K110689 | Inbody | Biospace Corporation Limited | 2011 | — |
| +1 | K123228 | Inbody 770, Inbody 570, Inbody S10, Inbody H20/Inbody H20(B) | Biospace Corporation Limited | 2013 | — |
| +1 | K141483 | Biospace Body Composition Analyzer | Biospace Corporation Limited | 2014 | — |
| +1 | K130777 | Inbody | Biospace Corporation Limited | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1994 | 1 | 0 |
| 2001 | 2 | 0 |
| 2002 | 1 | 0 |
| 2004 | 2 | 0 |
| 2006 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 2 | 0 |
| 2014 | 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 MNW? 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 MNW device
- #1 K231116 Multi-parameter detectorscore 11.4 · 14 generations · no Class I recall
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K052646 | Biospace Body Composition Analyzers, Models Inbody 520, 720 and S20Summary page 1…lnBodyJ3O; Classification Names: MNW ANALYZER, BODY COMPOSITION Common/Usual Name: Body fat meter 2. Equivalent legally marketed devices: The BioSpace InBodyS2O(K052646) and The RioSpace InBody27O(K092786) 3. Indications for Use (intended use) For use only in healthy subjects for Measurement o… | 2005 |
| * | K092786 | Inbody, Models: 270, R20, R20BSummary page 1…NW ANALYZER, BODY COMPOSITION Common/Usual Name: Body fat meter 2. Equivalent legally marketed devices: The BioSpace InBodyS2O(K052646) and The RioSpace InBody27O(K092786) 3. Indications for Use (intended use) For use only in healthy subjects for Measurement of: Estimated: Skeletal muscle mass,… | 2010 |
| * | — | BSM370 scale, stand-patient Named without a submission number |
What descends from it? (3)
3 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 28 years and passes through 3 companies; a new generation was cleared every 1.7 years on median.
- None of the 14 ancestors has a recall.
- Of its descendants, K123228 (Biospace Corporation Limited, 2013) has gone furthest, with 2 descendants of its own.
- 2 other devices also cite its predicate K052646.
How does its category compare?
All MNW devicesMNW Analyzer, Body Composition: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · MNW
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · MNW
110in 2014
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MNW
No recall names MNW since 2007.
Adverse event reports per year · MNW
3in 2024
MAUDE reports naming product code MNW, 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 | 4 | 109 | 0 | 0 |
| 2008 | 4 | 134 | 0 | 0 |
| 2009 | 4 | 137 | 0 | 0 |
| 2010 | 1 | — | 0 | 1 |
| 2011 | 11 | 168 | 0 | 0 |
| 2012 | 4 | 103 | 0 | 0 |
| 2013 | 9 | 144 | 0 | 0 |
| 2014 | 3 | 110 | 0 | 0 |
| 2015 | 1 | — | 0 | 2 |
| 2016 | 0 | — | 0 | 15 |
| 2017 | 0 | — | 0 | 6 |
| 2018 | 0 | — | 0 | 16 |
| 2019 | 0 | — | 0 | 11 |
| 2020 | 0 | — | 0 | 12 |
| 2021 | 0 | — | 0 | 10 |
| 2022 | 0 | — | 0 | 8 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 1 | — | 0 | 3 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
For use only in healthy subjects for Measurement of:
Estimated: Skeletal muscle mass, Extra-Cellular Water (ECW), Intra-Cellular Water (ICW),Total Body Water (TBW), Body Fat, Body Lean + Dry Lean, Metabolic Rates, Segmental Lean Mass, Segmental Body Fat mass, % Segmental Body Fat, and Energy expenditure of activity, Visceral Fat Area (yEA).
Actual : Weight [except for model S10, which requires the manual entry of weight], Body Mass Index (BMI), Impedance Values, height [only for model InBodyJ3O, which has height-meter function]
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K110689 · printed Nov 6, 2026
Cite this page
510(k) Report. “K110689: Inbody.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110689
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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