510(k) Report

510(k) · Cleared

Cleared

Xgeo GU60

K123105510(k) TraditionalCleared Jun 7, 2013248-day reviewClass II21 CFR 892.1680

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

Samsung Electronics Co., Ltd. · KPR System, X-Ray, Stationary

Cleared on Jun 7, 2013 as substantially equivalent to K102408 (DRGEM Corporation, 2010) and 1 other predicate after a 248-day review. Its family tree reaches back 7 generations to 1998.

Decided
Jun 7, 2013
Review
248 days
Class
Class II
Product code
KPR
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K981556 (1998). 18 ancestors in all, the oldest K862120 (1986). No later device cites it as a predicate yet.

  1. Root · 7 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 6 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 5 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 4 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. 3 generations backK042876 Urs LP Digital, Millennium, RadproSedecal., Sa. · 2004
  6. 2 generations backK090238 Sedecal X-Plus LP Plus Digital Diagnostic X-Ray SystemsSedecal., Sa. · 2009
  7. 1 generation backK102408 Digital Diagnostic X-Ray SystemDRGEM Corporation · 2010
  8. This deviceK123105 Xgeo GU60Samsung Electronics Co., Ltd. · 2013
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−6K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−5K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−4K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
−3K042876Urs LP Digital, Millennium, RadproSedecal., Sa.2004—
−2K090238Sedecal X-Plus LP Plus Digital Diagnostic X-Ray SystemsSedecal., Sa.2009—
−1K102408Digital Diagnostic X-Ray SystemDRGEM Corporation2010—
0 (this device)K123105Xgeo GU60Samsung Electronics Co., Ltd.2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198810
199810
199910
200010
200120
200210
200310
200620
FIG. 1 — Lineage of K123105, 1998–2013Source: 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 KPR? 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 KPR device

  1. #1 K242119 Innovision-Exiiscore 17.0 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K102408Digital Diagnostic X-Ray System
Summary page 1
…. Classification Name: System, X-ray, Stationary D. Product Code: KPR 6. Predicate Device A. Manufacturer: DRGEM Corporation B. Trade Name: Diamond-5A C. 510(k) Number: K102408 2/5 341 SAMSUNG ELECTRONICS Co., Ltd. 510(k) Premarket Notification - Traditional D. 510(k) Decision Date: 201…
DRGEM Corporation2010—
*K012389Revolution XR/D Digital Radiographic Imaging SystemGe Medical Systems, Inc.20014

Also cleared against K102408: 3 other devices →

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 15 years and passes through 5 companies; a new generation was cleared every 1.8 years on median.
  • 4 of the 18 ancestors have a recall of any class.
  • 3 other devices also cite its predicate K102408.

How does its category compare?

All KPR devices

KPR System, X-Ray, Stationary: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · KPR

8in 2025

2007: 122008: 152009: 92010: 92011: 92012: 112013: 52014: 102015: 182016: 112017: 62018: 152019: 122020: 162021: 62022: 82023: 92024: 112025: 82026 (partial year): 6
2007high 18 (2015) · low 5 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPR

155in 2025

2007: 31 days median2008: 48 days median2009: 35 days median2010: 126 days median2011: 152 days median2012: 58 days median2013: 163 days median2014: 108 days median2015: 81 days median2016: 84 days median2017: 75 days median2018: 30 days median2019: 33 days median2020: 39 days median2021: 55 days median2022: 43 days median2023: 76 days median2024: 162 days median2025: 155 days median2026 (partial year): 197 days median
2007high 197 (2026) · low 30 (2018)2026

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

Recalls per year · KPR

7in 2025

2007: 102008: 102009: 52010: 32011: 52012: 12013: 52014: 82015: 12016: 42017: 32018: 42019: 12020: 12022: 22023: 42024: 12025: 7
2007high 10 (2007) · low 0 (2021)2026

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

Adverse event reports per year · KPR

39in 2025

2007: 1202008: 952009: 612010: 822011: 1032012: 742013: 242014: 342015: 592016: 182017: 312018: 362019: 772020: 412021: 372022: 272023: 392024: 342025: 39
2007high 120 (2007) · low 18 (2016)2025

MAUDE reports naming product code KPR, 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
2007123110120
200815481095
2009935561
20109126382
201191525103
20121158174
20135163524
201410108834
20151881159
20161184418
2017675331
20181530436
20191233177
20201639141
2021655037
2022843227
2023976439
202411162134
20258155739
202661970—

What is it indicated for?

The XGEO GU60 Digital X-ray Imaging System is intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications.

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. “K123105: Xgeo GU60.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123105

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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