510(k) Report

510(k) · Cleared

Cleared

Lunar Astra

K252718510(k) TraditionalCleared Apr 20, 2026235-day reviewClass II21 CFR 892.1170

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 Apr 20, 2026 as substantially equivalent to K052581 (Ge Medical Systems Ultrasound and Primary Care Dia, 2005) and 1 other predicate after a 235-day review. Its family tree reaches back 8 generations to 1990.

Decided
Apr 20, 2026
Review
235 days
Class
Class II
Product code
KGI
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K890121 (1990). 45 ancestors in all, the oldest K883280 (1988). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2005: 1 other ancestor2016: 1 other ancestor2002: 2 other ancestors2000: 3 other ancestors1998: 6 other ancestors1992: 1 other ancestor2013: 1 other ancestor2012: 1 other ancestor2008: 2 other ancestors2007: 1 other ancestor1999: 3 other ancestors1995: 5 other ancestors1990: 2 other ancestors1989: 2 other ancestors2006: 1 other ancestor2001: 1 other ancestor1994: 1 other ancestor1996: 1 other ancestor1991: 1 other ancestor1988: 1 other ancestorK890121 · 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 · recalledK191112 · GEHC DXA Bone Densitometers with enCORE version 18 · GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC · 2019 · recalled1990200020102020
  1. Root · 8 generations backK890121 Modified DPX Bone DensitometerLunar · 1990
  2. 7 generations backK961007 Expert Spine Morphotietry ReferenceLunar Corp. · 1996
  3. 6 generations backK011917 Advanced Hip Assessment SoftwareGe Lunar Corp. · 2001
  4. 5 generations backK061561 Hip Structural Analysis Software Option for the Hologic QDR X-Ray…Hologic, Inc. · 2006
  5. 4 generations backK082402 Osdx Hip BMD SystemImaging Therapeutics, Inc. · 2008
  6. 3 generations backK121716 TBS InsightMedimaps Group SA · 2012
  7. 2 generations backK152299 TBS iNsightMedimaps Group SA · 2016 · Recalled
  8. 1 generation backK191112 GEHC DXA Bone Densitometers with enCORE version 18GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC · 2019 · Recalled
  9. This deviceK252718 Lunar AstraGE Medical Systems Ultrasound & Primary Care Diagnostics, LLC · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K890121Modified DPX Bone DensitometerLunar1990—
−7K961007Expert Spine Morphotietry ReferenceLunar Corp.1996—
−6K011917Advanced Hip Assessment SoftwareGe Lunar Corp.2001—
−5K061561Hip Structural Analysis Software Option for the Hologic QDR X-Ray Bone…Hologic, Inc.2006—
−4K082402Osdx Hip BMD SystemImaging Therapeutics, Inc.2008—
−3K121716TBS InsightMedimaps Group SA2012—
−2K152299TBS iNsightMedimaps Group SA20162
−1K191112GEHC DXA Bone Densitometers with enCORE version 18GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC20191
0 (this device)K252718Lunar AstraGE Medical Systems Ultrasound & Primary Care Diagnostics, LLC2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
198920
199020
199110
199210
199410
199550
199610
199860
199930
200030
200110
200220
200510
200610
200710
200820
201210
201310
201610
FIG. 1 — Lineage of K252718, 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 K254072 BoneVuescore 12.3 · 2 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
*K052581Lunar Idxa
Summary page 6
…ne densitometer Regulation: 21 CFR 892.1170 Classification: Class II Product Code: KGI Predicate Device: Lunar iDXA (K052581) 21 CFR 892.1170 (KGI) Class II Secondary Predicate GEHC DXA Bone…
Ge Medical Systems Ultrasound and Primary Care Dia20051
*K191112GEHC DXA Bone Densitometers with enCORE version 18
Summary page 6
…81) 21 CFR 892.1170 (KGI) Class II Secondary Predicate GEHC DXA Bone Densitometer with enCORE version 18 (K191112) Device: 21 CFR 892.1170 (KGI) Class II Manufacturing site: GE Hualun Med…
GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC20191

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 36 years and passes through 7 companies; a new generation was cleared every 5.0 years on median.
  • 6 of the 45 ancestors have a recall of any class.

How does its category compare?

All KGI devices

KGI Densitometer, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, 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?

The x-ray bone densitometer supports the following indications for use: 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…

Read the full statement (755 words)

The x-ray bone densitometer supports the following indications for use:

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.

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

F) Optional Vertebral Assessment Suite 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 Birth to 20 software 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 HealthCare 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 Neck to Knee software feature provides a complete bone and body composition assessment in one optimized exam including BMD, Fracture Risk, Adiposity/Metabolic status, and Sarcopenia status.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K252718: Lunar Astra.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K252718

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026