510(k) Report

510(k) · Cleared

Recalled · Class II · 2019

GEHC DXA Bone Densitometers with enCORE version 18

K191112510(k) TraditionalCleared Sep 19, 2019146-day reviewClass II21 CFR 892.1170Recalls 1

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

GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC · KGI Densitometer, Bone

Cleared on Sep 19, 2019 as substantially equivalent to K161682 (GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC, 2016) and 1 other predicate after a 146-day review. Its family tree reaches back 7 generations to 1990. 2 later devices descend from it. It has been recalled once.

Decided
Sep 19, 2019
Review
146 days
Class
Class II
Product code
KGI
Recalls
1
Predicates
2

Its longest line of descent runs back 7 generations to K890121 (1990). 34 ancestors in all, the oldest K883280 (1988). 2 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2016: 1 other ancestor2013: 1 other ancestor2012: 1 other ancestor2008: 2 other ancestors2007: 1 other ancestor2006: 1 other ancestor1998: 4 other ancestors1995: 4 other ancestors2002: 1 other ancestor2001: 1 other ancestor1999: 3 other ancestors1994: 1 other ancestor2000: 1 other ancestor1996: 1 other ancestor1991: 1 other ancestor1990: 1 other ancestor1989: 1 other ancestor1988: 1 other ancestor2025: 1 descendant cleared2026: 1 descendant clearedK890121 · Modified DPX Bone Densitometer · Lunar · 1990K961007 · Expert Spine Morphotietry Reference · Lunar Corp. · 1996K011917 · Advanced Hip Assessment Software · Ge Lunar Corp. · 2001K061561 · Hip Structural Analysis Software Option for the Hologic QDR X-Ray Bone Densitometers · Hologic, Inc. · 2006K082402 · Osdx Hip BMD System · Imaging Therapeutics, Inc. · 2008K121716 · TBS Insight · Medimaps Group SA · 2012K152299 · TBS iNsight · Medimaps Group SA · 2016 · recalled1990200020102020
  1. Root · 7 generations backK890121 Modified DPX Bone DensitometerLunar · 1990
  2. 6 generations backK961007 Expert Spine Morphotietry ReferenceLunar Corp. · 1996
  3. 5 generations backK011917 Advanced Hip Assessment SoftwareGe Lunar Corp. · 2001
  4. 4 generations backK061561 Hip Structural Analysis Software Option for the Hologic QDR X-Ray…Hologic, Inc. · 2006
  5. 3 generations backK082402 Osdx Hip BMD SystemImaging Therapeutics, Inc. · 2008
  6. 2 generations backK121716 TBS InsightMedimaps Group SA · 2012
  7. 1 generation backK152299 TBS iNsightMedimaps Group SA · 2016 · Recalled
  8. This deviceK191112 GEHC DXA Bone Densitometers with enCORE version 18GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC · 2019
  9. Descendant · cites it directly · 0 of its ownK252718 Lunar AstraGE Medical Systems Ultrasound & Primary Care Diagnostics, LLC · 2026
  10. Descendant · cites it directly · 0 of its ownK251022 3D-Shaper3D-Shaper Medical S.L · 2025

Most influential descendants

Showing 2 of 2 · See all
  • K252718Lunar AstraGE Medical Systems Ultrasound & Primary Care Diagnostics, LLC · 2026 · cites it directly0descendants
  • K2510223D-Shaper3D-Shaper Medical S.L · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K890121Modified DPX Bone DensitometerLunar1990—
−6K961007Expert Spine Morphotietry ReferenceLunar Corp.1996—
−5K011917Advanced Hip Assessment SoftwareGe Lunar Corp.2001—
−4K061561Hip Structural Analysis Software Option for the Hologic QDR X-Ray Bone…Hologic, Inc.2006—
−3K082402Osdx Hip BMD SystemImaging Therapeutics, Inc.2008—
−2K121716TBS InsightMedimaps Group SA2012—
−1K152299TBS iNsightMedimaps Group SA20162
0 (this device)K191112GEHC DXA Bone Densitometers with enCORE version 18GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC2019—
+1K252718Lunar AstraGE Medical Systems Ultrasound & Primary Care Diagnostics, LLC2026—
+1K2510223D-Shaper3D-Shaper Medical S.L2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
198910
199010
199110
199410
199540
199610
199840
199930
200010
200110
200210
200610
200710
200820
201210
201310
201610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
202610
FIG. 1 — Lineage of K191112, 1990–2026Source: 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 KGI? 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 KGI device

  1. #1 K252718 Lunar Astrascore 13.3 · 8 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
*K161682GE Lunar DXA Bone Densitometers with enCORE version 17
Summary page 6
…Predicate Device(s): 1. Lunar DXA Bone Densitometers with enCORE software: • GEHC DXA Bone Densitometer with enCORE version 17 (K161682) 2. MediMaps Group’s TBS Insight • TBS Insight (K152299) Device Des…
GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC20161
*K152299TBS iNsight
Summary page 6
…GEHC DXA Bone Densitometer with enCORE version 17 (K161682) 2. MediMaps Group’s TBS Insight • TBS Insight (K152299) Device Description: The changes proposed in this Premarket Notification will be used with the existing GE…
Medimaps Group SA20162

Also cleared against K161682: 1 other device →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K252718Lunar AstraGE Medical Systems Ultrasound & Primary Care Diagnostics, LLC20260
K2510223D-Shaper3D-Shaper Medical S.L20250

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Dec 3, 2019Class IIZ-1712-2020Radiation Control for Health and Safety ActAn issue with the Lunar iDXA control panel may cause the start button to not release and potentially contribute to an accidental radiation occurrence.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 29 years and passes through 7 companies; a new generation was cleared every 4.0 years on median.
  • 3 of the 34 ancestors have a recall of any class.
  • Of its descendants, K252718 (GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC, 2026) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K161682.

How does its category compare?

All KGI devices

KGI Densitometer, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · KGI

3in 2025

2007: 22008: 52009: 12011: 22012: 52013: 12014: 22016: 22018: 12019: 12022: 22023: 12025: 32026 (partial year): 2
2007high 5 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KGI

156in 2025

2008: 173 days median2012: 142 days median2025: 156 days median
2007high 173 (2008) · low 142 (2012)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · KGI

1in 2016

2008: 62009: 92011: 12016: 1
2007high 9 (2009) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · KGI

8in 2025

2008: 22009: 32011: 52012: 12013: 12014: 22016: 12017: 162018: 62020: 22021: 12022: 12023: 22024: 22025: 8
2007high 16 (2017) · low 0 (2007)2025

MAUDE reports naming product code KGI, 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
20072—00
2008517362
20091—93
20100—00
20112—15
2012514201
20131—01
20142—02
20150—00
20162—11
20170—016
20181—06
20191—00
20200—02
20210—01
20222—01
20231—02
20240—02
2025315608
20262—0—

What is it indicated for?

A) Provides an estimate of bone mineral density at various anatomical sites (Spine, Femur, Total Body, and Forearm). These values can then be compared to an adult reference population at the sole discretion of the physician. B) Provides an assessment of relative fracture risk based on the patient's T-score value using the categories of fracture risk defined by the World Health Organization (WHO). C) Provides an assessment of 10-year fracture risk using…

Read the full statement (1,028 words)

A) Provides an estimate of bone mineral density at various anatomical sites (Spine, Femur, Total Body, and Forearm). These values can then be compared to an adult reference population at the sole discretion of the physician.

B) Provides an assessment of relative fracture risk based on the patient's T-score value using the categories of fracture risk defined by the World Health Organization (WHO).

C) Provides an assessment of 10-year fracture risk using WHO FRAX model.

D) Provides a standardized bone density report using data from the densitometer and physician-generated assessments based on the patient's demographics, which can assist the physician in communicating scan results to the patient and the patient's referring physician. Optional Hand BMD software estimates the BMD at the hand.

E) Optional Hand BMD software estimates the BMD at the hand.

F) Optional Dual-Energy Vertebral Assessment software provides an x-ray image of the spine for qualitative visual assessment in order to identify vertebral deformations and estimate vertebral heights (morphometry).

G) Optional Orthopedic software estimates periprosthetic BMD of an orthopedic hip or knee implant (pre- and post-surgery).

H) Optional Complete Pediatric software option measures bone mineral content (BMC), bone mineral density (BMD) and body composition (lean body mass and fat mass) in patients from birth to 20 years of age. The software provides a comparison of measured variables obtained by dual energy x-ray absorptiometry to a database of reference values for patients 5-19 years of age. These data can be used for comparative purposes at the sole discretion of the physician. The software does not provide a reference population for comparative purposes for patients younger than 5 years of age.

I) Optional Body Composition software measures the regional and whole body bone mineral density (BMD), lean and fat tissue mass, and calculates other derivative values which can be displayed in user-defined statistical formats and trends and compared to reference populations at the sole discretion of the healthcare professional. Some of the diseases/conditions for which body composition values are useful include chronic renal failure, anorexia nervosa, obesity, AIDS/HIV, and cystic fibrosis.

J) The MirrorImage function used on the GE Lunar DXA bone densitometers can be used to estimate the total body composition and bone mineral density (BMD) when regions of the body are outside of the scan window by using scanned data from the corresponding region(s) on the opposite half of the body.

K) Optional CoreScan software estimates the Visceral Adipose Tissue (VAT) content and the Subcutaneous Adipose Tissue (SAT) content within the android region in a male or female population between the ages of 18 and 90 with a BMI between 18.5 and 40, excluding pregnant women. The content that is estimated is the VAT Mass, VAT Volume, VAT Area, SAT Mass, SAT Volume, and SAT Area. The values can be displayed in user-defined statistical formats and trends. Some of the diseases/conditions for which VAT estimation can be useful include hypertension, impaired fasting glucose, impaired glucose tolerance, diabetes mellitus, dyslipidemia, metabolic syndrome, and some cancers that are correlated to adipose tissue inflammation.

L) Optional total body composition software estimates the Resting Metabolic Rate (RMR) in the male or female population age 18 and older. The data can be displayed in user-defined statistical formats and trends.

M) Optional total body composition software estimates the Relative Skeletal Muscle Index (RSMI) in the male or female population age 18 and older. The data can be displayed in user-defined statistical formats and trends.

N) Optional Advanced Hip Assessment (AHA) software provides a measurement of hip axis length (HAL) and a mean value of HAL for Caucasian and Asian females on femur images. It also calculates hip geometry values used to evaluate the structural properties of the hip.

O) Optional Atypical Femur Fracture (AFF) software uses femur images to visualize focal reaction or thickening along the lateral cortex of the femoral shaft which may be accompanied by a transverse radiolucent line. This software provides measurements of the lateral and medial cortex width and quantifies focal thickening of the lateral cortex along the femoral shaft. The beaking index can be displayed and trended across serial scans.

P) Optional sarcopenia software calculates values based on published definitions and thresholds using measured appendicular lean mass in combination with patient demographics and entered values of muscle strength and physical performance. These values may be useful to health care professionals in their management of sarcopenia.

Q) Optional DXAVision software feature provides a complete bone and body composition assessment in one optimized exam including BMD with TBS, Fracture Risk, Adiposity/Metabolic status, and Sarcopenia status.

R) TBS iNsight is a software provided for use as a complement to both DXA analysis and clinical examination. It computes the antero-posterior spine DXA examination file and calculates a score (Trabecular Bone Score - TBS) that is compared to those of the age-matched controls. The TBS is derived from the texture of the DXA image and has been shown to be related to bone microarchitecture.

TBS iNsight provides as an option an assessment of 10-year fracture risk. It provides an estimate of 10-year probability of hip fracture and 10-year probability of a major osteoporotic fracture (clinical spine, forearm, hip or shoulder fracture). This estimate is based on the WHO’s FRAX® Fracture Risk Assessment Tool, after adjustment for the TBS. The tool has been validated for Caucasian and Asian men and post-menopausal women between 40 and 90 years old.

TBS provides information independent of BMD value; it is used as a complement to the data obtained from the DXA analysis and the clinical examination (questioning by the clinician about patient history, bioassay of bone resorption markers…). The results can be used by a physician in conjunction with other clinical risk factors as an aid in the diagnosis of osteoporosis and other medical conditions leading to altered trabecular bone microarchitecture, and ultimately in the assessment of fracture risk.

The TBS score can assist the health care professional in monitoring the effect of treatments on patients across time. Overall fracture risk will depend on many additional factors that should be considered before making diagnostic or therapeutic recommendations. The software does not diagnose disease or recommend treatment regimens. Only the health care professional can make these judgments.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K191112: GEHC DXA Bone Densitometers with enCORE version 18.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K191112

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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