510(k) Report

510(k) · Cleared

Cleared

Inbody 770, Inbody 570, Inbody S10, Inbody H20/Inbody H20(B)

K123228510(k) TraditionalCleared Mar 8, 2013144-day reviewClass II21 CFR 870.2770

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

Biospace Corporation Limited · MNW Analyzer, Body Composition

Cleared on Mar 8, 2013 as substantially equivalent to K110689 (Biospace Corporation Limited, 2011) after a 144-day review. Its family tree reaches back 7 generations to 1983. 2 later devices descend from it.

Decided
Mar 8, 2013
Review
144 days
Class
Class II
Product code
MNW
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K830292 (1983). 15 ancestors in all. 2 later devices descend from it, 2 citing it directly.

  1. Root · 7 generations backK830292 Bioelectrical Impedance Analyzer #101Rjl Systems, Inc. · 1983
  2. 6 generations backK023478 Inbody AP1 Body Composition AnalyzerBiospace Co.,Ltd · 2003
  3. 5 generations backK042528 Inbody, Model 3.0Biospace Corporation Limited · 2005
  4. 4 generations backK052646 Biospace Body Composition Analyzers, Models Inbody 520, 720 and S20Biospace Corporation Limited · 2005
  5. 3 generations backK062603 Biospace Body Composition Analyzers, Model Inbody 230Biospace Corporation Limited · 2007
  6. 2 generations backK092786 Inbody, Models: 270, R20, R20BBiospace Corporation Limited · 2010
  7. 1 generation backK110689 InbodyBiospace Corporation Limited · 2011
  8. This deviceK123228 Inbody 770, Inbody 570, Inbody S10, Inbody H20/Inbody H20(B)Biospace Corporation Limited · 2013
  9. Descendant · cites it directly · 0 of its ownK141483 Biospace Body Composition AnalyzerBiospace Corporation Limited · 2014
  10. Descendant · cites it directly · 0 of its ownK130777 InbodyBiospace Corporation Limited · 2013

Most influential descendants

Showing 2 of 2 · See all
  • 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

GenerationNumberDeviceApplicantDecidedRecalls
−7K830292Bioelectrical Impedance Analyzer #101Rjl Systems, Inc.1983—
−6K023478Inbody AP1 Body Composition AnalyzerBiospace Co.,Ltd2003—
−5K042528Inbody, Model 3.0Biospace Corporation Limited2005—
−4K052646Biospace Body Composition Analyzers, Models Inbody 520, 720 and S20Biospace Corporation Limited2005—
−3K062603Biospace Body Composition Analyzers, Model Inbody 230Biospace Corporation Limited2007—
−2K092786Inbody, Models: 270, R20, R20BBiospace Corporation Limited2010—
−1K110689InbodyBiospace Corporation Limited2011—
0 (this device)K123228Inbody 770, Inbody 570, Inbody S10, Inbody H20/Inbody H20(B)Biospace Corporation Limited2013—
+1K141483Biospace Body Composition AnalyzerBiospace Corporation Limited2014—
+1K130777InbodyBiospace Corporation Limited2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
200120
200210
200420
200620

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
201410
FIG. 1 — Lineage of K123228, 1983–2014Source: 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 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. #1 K231116 Multi-parameter detectorscore 11.4 · 14 generations · no Class I recall
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K110689Inbody
Summary page 1
…ication: 11 2. Equivalent legally marketed devices: (Predicate device Information) Biospace Body Composition Analyzer Model lnBodyl7O, Model lnBodyJ3O InBodySlO K110689 3. Indications for Use lnBody77O, InBody57O, InBody S10, InBody H20/lnBody H208 For use only in healthy subjects fo…
Biospace Corporation Limited2011—

Also cleared against K110689: 2 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K141483Biospace Body Composition AnalyzerBiospace Corporation Limited20140
K130777InbodyBiospace Corporation Limited20130

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 30 years and passes through 3 companies; a new generation was cleared every 1.6 years on median.
  • None of the 15 ancestors has a recall.
  • Of its descendants, K141483 (Biospace Corporation Limited, 2014) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K110689.

How does its category compare?

All MNW devices

MNW Analyzer, Body Composition: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · MNW

1in 2024

2007: 42008: 42009: 42010: 12011: 112012: 42013: 92014: 32015: 12024: 1
2007high 11 (2011) · low 0 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MNW

110in 2014

2007: 109 days median2008: 134 days median2009: 137 days median2011: 168 days median2012: 103 days median2013: 144 days median2014: 110 days median
2007high 168 (2011) · low 103 (2012)2026

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

2010: 12015: 22016: 152017: 62018: 162019: 112020: 122021: 102022: 82023: 22024: 3
2007high 16 (2018) · low 0 (2007)2025

MAUDE reports naming product code MNW, 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
2007410900
2008413400
2009413700
20101—01
20111116800
2012410300
2013914400
2014311000
20151—02
20160—015
20170—06
20180—016
20190—011
20200—012
20210—010
20220—08
20230—02
20241—03
20250—00
20260—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), ECW/TBW, Body Fat Percentage of Body Fat (PBF), BodyLean + Dry Lean, Metabolic Rates(Basal Metabolic Rates), Segmental Lean Mass, Segmental Fat Mass, % Segmental Body Fat, Energy Expenditure of Activity, Visceral Fat Area (VFA),.Visceral Fat Level, Segmental Body Water, Body Shape Graph…

Read the full statement (143 words)

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), ECW/TBW, Body Fat Percentage of Body Fat (PBF), BodyLean + Dry Lean, Metabolic Rates(Basal Metabolic Rates), Segmental Lean Mass, Segmental Fat Mass, % Segmental Body Fat, Energy Expenditure of Activity, Visceral Fat Area (VFA),.Visceral Fat Level, Segmental Body Water, Body Shape Graph

Actual: Weight (except for Model InBodyS 10, which requires the manual entry of weight], Body Mass Index (BMI) and Impedance Values, Height [except for Model InBody S1 and InBody H2OIInBody 1120(l1), which requires the manual entry of Height], Resistance Values [only for InBody77O, Inflody S 10], Reactance Values (for InBody77O, InBody 510], Phase Angle [for InBody77O, InBody S10]. The InBody R120 and the InBody R20® are identical except that the @E model has Bluetooth capability for data transfer.

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. “K123228: Inbody 770, Inbody 570, Inbody S10, Inbody H20/Inbody H20(B).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123228

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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