510(k) · Cleared
ClearedKrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medicatech USA · KPR System, X-Ray, Stationary
Cleared on Feb 6, 2015 as substantially equivalent to K133782 (Sedecal., Sa., 2014) after an 85-day review. Its family tree reaches back 7 generations to 1998. 2 later devices descend from it.
- Decided
- Feb 6, 2015
- Review
- 85 days
- Class
- Class II
- Product code
- KPR
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 7 generations to K981556 (1998). 11 ancestors in all. 2 later devices descend from it, 2 citing it directly.
- Root · 7 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
- 6 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
- 5 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
- 4 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
- 3 generations backK042876 Urs LP Digital, Millennium, RadproSedecal., Sa. · 2004
- 2 generations backK090279 Sedecal, Millennium PlusSedecal., Sa. · 2009
- 1 generation backK133782 Nova FA DR SystemSedecal., Sa. · 2014 · Recalled
- This deviceK143257 KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic…Medicatech USA · 2015
- Descendant · cites it directly · 0 of its ownK190601 MasteRad MX30Medicatech USA · 2019
- Descendant · cites it directly · 0 of its ownK151219 Models 2200DR and 1600DR Digital Stationary Radiographic SystemsBeijing Polycon Medical Engineering Company · 2015
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K981556 | Canon X-Ray Digital Camera Cxdi-11 | Canon USA, Inc. | 1998 | — |
| −6 | K992547 | Canon X-Ray Digital Camera, Model Cxdi-22 | Canon USA, Inc. | 1999 | — |
| −5 | K023750 | Cannon Digital Radiography Model Cxdi-40G | Canon USA, Inc. | 2002 | — |
| −4 | K031447 | Canon, Digital Radiography, Model Cxdi-50G | Canon, Inc. | 2003 | — |
| −3 | K042876 | Urs LP Digital, Millennium, Radpro | Sedecal., Sa. | 2004 | — |
| −2 | K090279 | Sedecal, Millennium Plus | Sedecal., Sa. | 2009 | — |
| −1 | K133782 | Nova FA DR System | Sedecal., Sa. | 2014 | 1 |
| 0 (this device) | K143257 | KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System | Medicatech USA | 2015 | — |
| +1 | K190601 | MasteRad MX30 | Medicatech USA | 2019 | — |
| +1 | K151219 | Models 2200DR and 1600DR Digital Stationary Radiographic Systems | Beijing Polycon Medical Engineering Company | 2015 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 1 | 0 |
| 2001 | 1 | 0 |
| 2002 | 1 | 0 |
| 2006 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 1 | 0 |
| 2019 | 1 | 0 |
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 K242119 Innovision-Exiiscore 17.0 · 9 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K133782 | Nova FA DR SystemSummary page 4…Product codes KPR and MQB Common/Usual Name: Digital Diagnositc X-Ray System Device Class: II per regulation 21CFR892.1680 2. Equivalent legally marketed device: K133782, Sedecal Nova FA DR System, Sedecal SA. 3. Indications for Use The KrystalRad 1100 and KrystalRad 3000 Digital Stationary Radiog… | 2014 |
| † | K103591 | Digital Radiography | 2011 |
| † | K091436 | Digital Radiography, Model Cxdi-55C | 2009 |
| † | K111682 | Digital Radiography | 2011 |
| † | K130337 | Randox Speciality Control (I) Levels 1, 2 and 3 | 2013 |
| † | K130883 | Sedecal Digital Radiographic Upgrade Model Sdru-T | 2013 |
| † | K140825 | Delworks DR System | 2014 |
| † | K131121 | Full Automatic (Nibp) Blood Pressure Monitor | 2013 |
| † | K140551 | Perkinelmer, Xrpad 4336 Med Flat Panel Detector | 2014 |
| † | K090238 | Sedecal X-Plus LP Plus Digital Diagnostic X-Ray Systems | 2009 |
What descends from it? (2)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 17 years and passes through 4 companies; a new generation was cleared every 1.5 years on median.
- 2 of the 11 ancestors have a recall of any class.
- Of its descendants, K190601 (Medicatech USA, 2019) has gone furthest, with 0 descendants of its own.
- 4 other devices also cite its predicate K133782.
How does its category compare?
All KPR devicesKPR System, X-Ray, Stationary: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · KPR
8in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KPR
155in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KPR
7in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KPR
39in 2025
MAUDE reports naming product code KPR, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 12 | 31 | 10 | 120 |
| 2008 | 15 | 48 | 10 | 95 |
| 2009 | 9 | 35 | 5 | 61 |
| 2010 | 9 | 126 | 3 | 82 |
| 2011 | 9 | 152 | 5 | 103 |
| 2012 | 11 | 58 | 1 | 74 |
| 2013 | 5 | 163 | 5 | 24 |
| 2014 | 10 | 108 | 8 | 34 |
| 2015 | 18 | 81 | 1 | 59 |
| 2016 | 11 | 84 | 4 | 18 |
| 2017 | 6 | 75 | 3 | 31 |
| 2018 | 15 | 30 | 4 | 36 |
| 2019 | 12 | 33 | 1 | 77 |
| 2020 | 16 | 39 | 1 | 41 |
| 2021 | 6 | 55 | 0 | 37 |
| 2022 | 8 | 43 | 2 | 27 |
| 2023 | 9 | 76 | 4 | 39 |
| 2024 | 11 | 162 | 1 | 34 |
| 2025 | 8 | 155 | 7 | 39 |
| 2026 | 6 | 197 | 0 | — |
What is it indicated for?
The KrystalRad 1100 and KrystalRad 3000 Digital Stationary Radiographic Systems are intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest. abdomen, extremities, and other body parts. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position. Not for mammography.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K143257 · printed Nov 5, 2026
Cite this page
510(k) Report. “K143257: KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K143257
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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