510(k) · Cleared
ClearedSensus Healthcare Superficial Radiotherapy System SRT-100
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sensus Healthcare · JAD System, Therapeutic, X-Ray
Cleared on May 14, 2013 as substantially equivalent to K063456 (Topex, Inc., 2007) and 2 other predicates after a 139-day review. Its family tree reaches back 2 generations to 1996. 7 later devices descend from it.
- Decided
- May 14, 2013
- Review
- 139 days
- Class
- Class II
- Product code
- JAD
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 2 generations to K962613 (1996). 3 ancestors in all. 7 later devices descend from it, 2 citing it directly.
- Root · 2 generations backK962613 Darpac 2000 Superficial X-Ray Therapy SystemGulmay Medical, Ltd. · 1996 · Recalled
- 1 generation backK063456 SRT100 Superficial Radiation Therapy SystemTopex, Inc. · 2007
- This deviceK123985 Sensus Healthcare Superficial Radiotherapy System SRT-100Sensus Healthcare · 2013
- Descendant · cites it directly · 4 of its ownK131582 Sensus Helthcare Image-Duided Superficial Radiotherapy SystemSensus Healthcare · 2013
- Descendant · 2 generations on · 3 of its ownK150037 Sensus Healthcare Superficial X-ray Radiation Therapy System with…Sensus Healthcare · 2015 · Recalled
- Descendant · cites it directly · 1 of its ownK172080 Photoelectric Therapy SystemXstrahl, Ltd. · 2017 · Recalled
- Descendant · 3 generations on · 0 of its ownK250692 GentleBeam (GB1000)Voxel Ray Solutions, LLC · 2025
- Descendant · 2 generations on · 0 of its ownK230611 X80 / RADiant / PhotoElectric Therapy System (RADiant Aura)Xstrahl, Ltd. · 2023
Showing 5 of 7 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 7 · See all- K131582Sensus Helthcare Image-Duided Superficial Radiotherapy SystemSensus Healthcare · 2013 · cites it directly4descendants
- K150037Sensus Healthcare Superficial X-ray Radiation Therapy System with Ultrasonic Imaging…Sensus Healthcare · 2015 · 2 generations on3descendants
- K172080Photoelectric Therapy SystemXstrahl, Ltd. · 2017 · cites it directly1descendant
- K250692GentleBeam (GB1000)Voxel Ray Solutions, LLC · 2025 · 3 generations on0descendants
- K230611X80 / RADiant / PhotoElectric Therapy System (RADiant Aura)Xstrahl, Ltd. · 2023 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K962613 | Darpac 2000 Superficial X-Ray Therapy System | Gulmay Medical, Ltd. | 1996 | 2 |
| −1 | K063456 | SRT100 Superficial Radiation Therapy System | Topex, Inc. | 2007 | — |
| 0 (this device) | K123985 | Sensus Healthcare Superficial Radiotherapy System SRT-100 | Sensus Healthcare | 2013 | — |
| +1 | K131582 | Sensus Helthcare Image-Duided Superficial Radiotherapy System | Sensus Healthcare | 2013 | — |
| +2 | K150037 | Sensus Healthcare Superficial X-ray Radiation Therapy System with Ultrasonic… | Sensus Healthcare | 2015 | 1 |
| +1 | K172080 | Photoelectric Therapy System | Xstrahl, Ltd. | 2017 | 2 |
| +3 | K250692 | GentleBeam (GB1000) | Voxel Ray Solutions, LLC | 2025 | — |
| +2 | K230611 | X80 / RADiant / PhotoElectric Therapy System (RADiant Aura) | Xstrahl, Ltd. | 2023 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
| 2015 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2022 | 1 | 0 |
| 2023 | 1 | 0 |
| 2025 | 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 JAD? 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 JAD device
- #1 K241174 INTRABEAM (700); And accessories (INTRABEAM…score 11.7 · 11 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (4)
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 |
|---|---|---|---|
| * | K063456 | SRT100 Superficial Radiation Therapy System | 2007 |
| * | K971074 | Therapax SXT 150Summary page 1…6 34 56 )*Nee Pantak Superficial X-ray Therapy System (K97 1074) Gulmay D31I00/Xstrahl 100… | 1997 |
| * | K962613 | Darpac 2000 Superficial X-Ray Therapy SystemSummary page 1…System (K97 1074) Gulmay D31I00/Xstrahl 100 (K962613) ORIGINAL Section 5 -510(k) Summary (Sensus Healthcare SRT-iO0)… | 1996 |
| * | — | Philips RT 100 Named without a submission number |
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 17 years and passes through 3 companies; a new generation was cleared every 10.3 years on median.
- 1 of the 3 ancestors has a recall of any class.
- Of its descendants, K131582 (Sensus Healthcare, 2013) has gone furthest, with 4 descendants of its own.
- 1 other device also cites its predicate K063456.
How does its category compare?
All JAD devicesJAD System, Therapeutic, X-Ray: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · JAD
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JAD
114in 2013
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JAD
2in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JAD
1in 2025
MAUDE reports naming product code JAD, 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 | 2 |
| 2008 | 2 | — | 0 | 2 |
| 2009 | 3 | 106 | 2 | 5 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 1 | — | 1 | 3 |
| 2012 | 2 | — | 3 | 4 |
| 2013 | 5 | 114 | 0 | 12 |
| 2014 | 1 | — | 0 | 4 |
| 2015 | 1 | — | 0 | 5 |
| 2016 | 2 | — | 0 | 5 |
| 2017 | 1 | — | 1 | 3 |
| 2018 | 1 | — | 0 | 1 |
| 2019 | 2 | — | 0 | 9 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 2 | 0 |
| 2022 | 1 | — | 0 | 5 |
| 2023 | 1 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 5 |
| 2025 | 2 | — | 0 | 1 |
| 2026 | 0 | — | 1 | — |
What is it indicated for?
The SRT-100 is a low energy X-ray system intended for superficial radiotherapy treatment of primary malignant epithelial neoplasms of the skin and keloids. Applications include basal cell carcinoma, squamous cell carcinoma, Metatypic carcinoma, cutaneous appendage carcinoma, Karposi's Sarcoma, and the treatment of keloids. Keloids are benign fibrous growths that arise from proliferation of dermal tissue typically arising from injuries to skin tissue.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K123985 · printed Nov 5, 2026
Cite this page
510(k) Report. “K123985: Sensus Healthcare Superficial Radiotherapy System SRT-100.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K123985
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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