510(k) · Cleared
ClearedPortable X-ray System (Model: MINIX-V / MINIX-S)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012) · EHD Unit, X-Ray, Extraoral With Timer
Cleared on Dec 3, 2015 as substantially equivalent to K063121 (Genoray Co., Ltd., 2007) and 2 other predicates after a 64-day review. Its family tree reaches back 5 generations to 2000. 7 later devices descend from it.
- Decided
- Dec 3, 2015
- Review
- 64 days
- Class
- Class II
- Product code
- EHD
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 5 generations to K000061 (2000). 6 ancestors in all. 7 later devices descend from it, 2 citing it directly.
- Root · 5 generations backK000061 Minxray HF70D High Frequency Portable Dental X-Ray UnitMinxray, Inc. · 2000
- 4 generations backK021378 Portable HDX Intraoral X-RayDentalez Group · 2002 · Recalled
- 3 generations backK051795 Nomad Dental X-Ray SystemAribex, Inc. · 2005
- 2 generations backK063121 Portable X-Ray System, Model Port-X IIGenoray Co., Ltd. · 2007
- 1 generation backK082167 Portable X-Ray System, Models Diox-602, ProxDigimed Corporation · 2008 · Recalled
- This deviceK152859 Portable X-ray System (Model: MINIX-V / MINIX-S)Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012) · 2015
- Descendant · cites it directly · 5 of its ownK180561 MobileX Portable X-ray SystemDenterprise International, Inc. · 2018
- Descendant · 2 generations on · 2 of its ownK232068 HyperLight Portable X-ray UnitChangzhou Sifary Medical Technology Co., Ltd. · 2023
- Descendant · 2 generations on · 1 of its ownK231449 Portable X-ray System Model Ray98(P)Ningbo Runyes Medical Instrument Co., Ltd. · 2023
- Descendant · 3 generations on · 0 of its ownK260795 Hand-held Dental X-ray System (HyperLight-M)Changzhou Sifary Medical Technology Co., Ltd. · 2026
- Descendant · 3 generations on · 0 of its ownK254018 Portable Dental X-ray Device (GT-1)Guilin Refine Medical Instrument Co., Ltd. · 2026
Showing 5 of 7 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 7 · See all- K180561MobileX Portable X-ray SystemDenterprise International, Inc. · 2018 · cites it directly5descendants
- K232068HyperLight Portable X-ray UnitChangzhou Sifary Medical Technology Co., Ltd. · 2023 · 2 generations on2descendants
- K231449Portable X-ray System Model Ray98(P)Ningbo Runyes Medical Instrument Co., Ltd. · 2023 · 2 generations on1descendant
- K260795Hand-held Dental X-ray System (HyperLight-M)Changzhou Sifary Medical Technology Co., Ltd. · 2026 · 3 generations on0descendants
- K254018Portable Dental X-ray Device (GT-1)Guilin Refine Medical Instrument Co., Ltd. · 2026 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K000061 | Minxray HF70D High Frequency Portable Dental X-Ray Unit | Minxray, Inc. | 2000 | — |
| −4 | K021378 | Portable HDX Intraoral X-Ray | Dentalez Group | 2002 | 1 |
| −3 | K051795 | Nomad Dental X-Ray System | Aribex, Inc. | 2005 | — |
| −2 | K063121 | Portable X-Ray System, Model Port-X II | Genoray Co., Ltd. | 2007 | — |
| −1 | K082167 | Portable X-Ray System, Models Diox-602, Prox | Digimed Corporation | 2008 | 1 |
| 0 (this device) | K152859 | Portable X-ray System (Model: MINIX-V / MINIX-S) | Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012) | 2015 | — |
| +1 | K180561 | MobileX Portable X-ray System | Denterprise International, Inc. | 2018 | — |
| +2 | K232068 | HyperLight Portable X-ray Unit | Changzhou Sifary Medical Technology Co., Ltd. | 2023 | — |
| +2 | K231449 | Portable X-ray System Model Ray98(P) | Ningbo Runyes Medical Instrument Co., Ltd. | 2023 | — |
| +3 | K260795 | Hand-held Dental X-ray System (HyperLight-M) | Changzhou Sifary Medical Technology Co., Ltd. | 2026 | — |
| +3 | K254018 | Portable Dental X-ray Device (GT-1) | Guilin Refine Medical Instrument Co., Ltd. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 2 | 0 |
| 2023 | 2 | 0 |
| 2026 | 3 | 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 EHD? 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 EHD device
- #1 K260795 Hand-held Dental X-ray System (HyperLight-M)score 14.1 · 8 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K063121 | Portable X-Ray System, Model Port-X IISummary page 4…regulation 21CFR 872.1800 regulation 21CFR 872.1800 K103600 - BIOX K063121 (Decision Date: Mar. 10, 2011) 510(k) Number: (Decision Date: Ja… | 2007 |
| * | K103600 | Portable X-Ray SystemSummary page 4…I per System: EHD, Class II per regulation 21CFR 872.1800 regulation 21CFR 872.1800 K103600 - BIOX K063121 (Decision Date: Mar. 10, 2011)… | 2011 |
| * | K082167 | Portable X-Ray System, Models Diox-602, ProxSummary page 4…(Decision Date: Mar. 10, 2011) 510(k) Number: (Decision Date: Jan. 11, 2007) K082167 - PROX / DIOX-602 (Decision Date: July 29, 2008)… | 2008 |
What descends from it? (7)
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 15 years and passes through 6 companies; a new generation was cleared every 2.2 years on median.
- 2 of the 6 ancestors have a recall of any class.
- Of its descendants, K180561 (Denterprise International, Inc., 2018) has gone furthest, with 5 descendants of its own.
- 6 other devices also cite its predicate K063121.
How does its category compare?
All EHD devicesEHD Unit, X-Ray, Extraoral With Timer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · EHD
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · EHD
58in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · EHD
1in 2017
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · EHD
6in 2024
MAUDE reports naming product code EHD, 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 | 1 | — | 0 | 5 |
| 2008 | 5 | 49 | 0 | 6 |
| 2009 | 4 | 92 | 0 | 38 |
| 2010 | 4 | 268 | 3 | 47 |
| 2011 | 3 | 102 | 3 | 26 |
| 2012 | 2 | — | 0 | 22 |
| 2013 | 4 | 216 | 0 | 21 |
| 2014 | 3 | 107 | 1 | 20 |
| 2015 | 1 | — | 0 | 110 |
| 2016 | 2 | — | 1 | 63 |
| 2017 | 4 | 28 | 1 | 66 |
| 2018 | 5 | 30 | 0 | 21 |
| 2019 | 4 | 173 | 0 | 21 |
| 2020 | 2 | — | 0 | 4 |
| 2021 | 1 | — | 0 | 4 |
| 2022 | 8 | 58 | 0 | 4 |
| 2023 | 8 | 147 | 0 | 2 |
| 2024 | 7 | 58 | 0 | 6 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 6 | 128 | 0 | — |
What is it indicated for?
The device is a diagnostic X-ray system, which is intended to be used by trained dentists and dental technicians as an
extra-oral X-ray source for producing diagnostic X-ray images using intra-oral image receptors. Its use is intended for
both adults and pediatric subjects.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K152859 · printed Nov 6, 2026
Cite this page
510(k) Report. “K152859: Portable X-ray System (Model: MINIX-V / MINIX-S).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K152859
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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