510(k) Report

510(k) · Cleared

Cleared

GXR-Series Diagnostic X-Ray System

K202572510(k) SpecialCleared Sep 24, 202020-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

DRGEM Corporation · KPR System, X-Ray, Stationary

Cleared on Sep 24, 2020 as substantially equivalent to K192364 (DRGEM Corporation, 2019) after a 20-day review. Its family tree reaches back 8 generations to 1998. 8 later devices descend from it.

Decided
Sep 24, 2020
Review
20 days
Class
Class II
Product code
KPR
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K981556 (1998). 14 ancestors in all. 8 later devices descend from it, 4 citing it directly.

  1. Root · 8 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 7 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 6 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 5 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. 4 generations backK042876 Urs LP Digital, Millennium, RadproSedecal., Sa. · 2004
  6. 3 generations backK090238 Sedecal X-Plus LP Plus Digital Diagnostic X-Ray SystemsSedecal., Sa. · 2009
  7. 2 generations backK102408 Digital Diagnostic X-Ray SystemDRGEM Corporation · 2010
  8. 1 generation backK192364 GXR-Series Diagnostic X-Ray SystemDRGEM Corporation · 2019
  9. This deviceK202572 GXR-Series Diagnostic X-Ray SystemDRGEM Corporation · 2020
  10. Descendant · cites it directly · 2 of its ownK242119 Innovision-ExiiDk Medical System · 2025
  11. Descendant · cites it directly · 2 of its ownK233530 EXSYS DEXi (EXSYS DEXi-D401S-FRM); EXSYS DEXi (EXSYS…DRTECH Corporation · 2024
  12. Descendant · 2 generations on · 1 of its ownK242847 EXSYS DEXi (EXSYS DEXi-D401S-FRM); EXSYS DEXi (EXSYS…DRTECH Corporation · 2024
  13. Descendant · 3 generations on · 0 of its ownK260227 EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS…DRTECH Corporation · 2026
  14. Descendant · 2 generations on · 0 of its ownK253446 AeroDR TX c02Dk Medical Systems Co., Ltd. · 2026

Showing 5 of 8 descendants. See all descendants

Descendants cleared per year

2023: 12024: 22025: 32026: 2
2023high 3 (2025) · low 1 (2023)2026

Most influential descendants

Showing 5 of 8 · See all
  • K242119Innovision-ExiiDk Medical System · 2025 · cites it directly2descendants
  • K233530EXSYS DEXi (EXSYS DEXi-D401S-FRM); EXSYS DEXi (EXSYS DEXi-A401S-FRM); EXSYS DEXi (EXSYS…DRTECH Corporation · 2024 · cites it directly2descendants
  • K242847EXSYS DEXi (EXSYS DEXi-D401S-FRM); EXSYS DEXi (EXSYS DEXi-A401S-FRM); EXSYS DEXi (EXSYS…DRTECH Corporation · 2024 · 2 generations on1descendant
  • K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS…DRTECH Corporation · 2026 · 3 generations on0descendants
  • K253446AeroDR TX c02Dk Medical Systems Co., Ltd. · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−7K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−6K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−5K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
−4K042876Urs LP Digital, Millennium, RadproSedecal., Sa.2004—
−3K090238Sedecal X-Plus LP Plus Digital Diagnostic X-Ray SystemsSedecal., Sa.2009—
−2K102408Digital Diagnostic X-Ray SystemDRGEM Corporation2010—
−1K192364GXR-Series Diagnostic X-Ray SystemDRGEM Corporation2019—
0 (this device)K202572GXR-Series Diagnostic X-Ray SystemDRGEM Corporation2020—
+1K242119Innovision-ExiiDk Medical System2025—
+1K233530EXSYS DEXi (EXSYS DEXi-D401S-FRM); EXSYS DEXi (EXSYS DEXi-A401S-FRM); EXSYS…DRTECH Corporation2024—
+2K242847EXSYS DEXi (EXSYS DEXi-D401S-FRM); EXSYS DEXi (EXSYS DEXi-A401S-FRM); EXSYS…DRTECH Corporation2024—
+3K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS…DRTECH Corporation2026—
+2K253446AeroDR TX c02Dk Medical Systems Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010
200110
200210
200310
200620

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
202420
202530
202620
FIG. 1 — Lineage of K202572, 1998–2026Source: 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 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
Get a 510(k) Report

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
*K192364GXR-Series Diagnostic X-Ray System
Summary page 4
…KPR Regulation number: 892.1680 Regulatory Class: II III. PREDICATE DEVICE Product Name: GXR-Series Diagnostic X-Ray System Submission Number: K192364 Decision Date: 09/26/2019 Common Name: Digital Diagnostic X-ray System Regulation Name: Stationary…
DRGEM Corporation2019—

Also cleared against K192364: 2 other devices →

What descends from it? (8)

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

NumberDeviceApplicantDecidedDescendants
K242119Innovision-ExiiDk Medical System20252
K233530EXSYS DEXi (EXSYS DEXi-D401S-FRM); EXSYS DEXi (EXSYS DEXi-A401S-FRM); EXSYS DEXi (EXSYS…DRTECH Corporation20242
K242019GXR-Series Diagnostic X-Ray SystemDRGEM Corporation20250
K232178GXR-ES/ECS Diagnostic X-Ray System, (Models GXR-ES series, GXR-ECS series)DRGEM Corporation20230

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 22 years and passes through 4 companies; a new generation was cleared every 1.8 years on median.
  • 1 of the 14 ancestors has a recall of any class.
  • Of its descendants, K242119 (Dk Medical System, 2025) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K192364.

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. 2020, 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?

GXR-Series Diagnostic X-Ray System, is a stationary X-ray imaging system, for the purpose of acquiring X-ray images of the desired parts of a patient’s anatomy. This device is not intended for mammography or bone density 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. “K202572: GXR-Series Diagnostic X-Ray System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202572

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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