510(k) Report

510(k) · Cleared

Cleared

TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1)

K232870510(k) TraditionalCleared Dec 21, 202397-day reviewClass II21 CFR 892.5050

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

Varian Medical Systems, Inc. · IYE Accelerator, Linear, Medical

Cleared on Dec 21, 2023 as substantially equivalent to K231317 (Varian Medical Systems, Inc., 2023) after a 97-day review. Its family tree reaches back 14 generations to 1995. 1 later device descends from it.

Decided
Dec 21, 2023
Review
97 days
Class
Class II
Product code
IYE
Recalls
None
Predicates
1

Its longest line of descent runs back 14 generations to K926449 (1995). 39 ancestors in all, the oldest K864886 (1987). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2017: 1 other ancestor2013: 1 other ancestor2010: 1 other ancestor2012: 1 other ancestor1999: 1 other ancestor2008: 2 other ancestors1987: 1 other ancestor2007: 2 other ancestors2006: 2 other ancestors2004: 3 other ancestors2001: 1 other ancestor1996: 2 other ancestors2005: 1 other ancestor2003: 2 other ancestors2000: 2 other ancestors1997: 1 other ancestor1991: 1 other ancestor2025: 1 descendant clearedK926449 · Varian Multileaf Collimator, Release 4.0 · Varian Assoc., Inc. · 1995K973889 · Varian Multileaf Collimator with Dynamic Arc Therapy Feature · Varian Medical Systems, Inc. · 1997K990085 · Millennium MLC -120 · Varian Assoc., Inc. · 1999 · recalledK050442 · Millennium Multi-Leaf Collimator · Varian Medical Systems · 2005 · recalledK071992 · High-Definition 120 Multileaf Collimator (HD120 MLC) · Varian Medical Systems · 2007 · recalledK092871 · Trilogy MX · Varian Medical Systems, Inc. · 2009 · recalledK111106 · Truebeam · Varian Medical Systems, Inc. · 2011 · recalledK123291 · Truebeam · Varian Medical Systems, Inc. · 2012×2: 2 generations cleared close together, K140528 (2014), K143224 (2014) K162472 · TrueBeam-TrueBeam STx-Edge · Varian Medical Systems, Inc. · 2017K171733 · TrueBeam, TrueBeam STx, Edge · Varian Medical Systems, Inc. · 2017K213977 · TrueBeam, TrueBeam STx, Edge, VitalBeam · Varian Medical Systems, Inc. · 2022K231317 · TrueBeam, TrueBeam STx, Edge, VitalBeam · Varian Medical Systems, Inc. · 20231990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 1 other ancestor7 generations back: 2 other ancestors8 generations back: 2 other ancestors9 generations back: 2 other ancestors10 generations back: 6 other ancestors11 generations back: 3 other ancestors12 generations back: 4 other ancestors13 generations back: 5 other ancestors 1 generation forward: 1 descendant K231317 · TrueBeam, TrueBeam STx, Edge, VitalBeam · Varian Medical Systems, Inc. · 2023K213977 · TrueBeam, TrueBeam STx, Edge, VitalBeam · Varian Medical Systems, Inc. · 2022K171733 · TrueBeam, TrueBeam STx, Edge · Varian Medical Systems, Inc. · 2017K162472 · TrueBeam-TrueBeam STx-Edge · Varian Medical Systems, Inc. · 2017K143224 · TrueBeam-TrueBeam STx-Edge · Varian Medical Systems, Inc. · 2014 · recalledK140528 · True Beam, True Beam STX, Edge · Varian Medical Systems, Inc. · 2014 · recalledK123291 · Truebeam · Varian Medical Systems, Inc. · 2012K111106 · Truebeam · Varian Medical Systems, Inc. · 2011 · recalledK092871 · Trilogy MX · Varian Medical Systems, Inc. · 2009 · recalledK071992 · High-Definition 120 Multileaf Collimator (HD120 MLC) · Varian Medical Systems · 2007 · recalledK050442 · Millennium Multi-Leaf Collimator · Varian Medical Systems · 2005 · recalledK990085 · Millennium MLC -120 · Varian Assoc., Inc. · 1999 · recalledK973889 · Varian Multileaf Collimator with Dynamic Arc Therapy Feature · Varian Medical Systems, Inc. · 1997K926449 · Varian Multileaf Collimator, Release 4.0 · Varian Assoc., Inc. · 1995−10−50
  1. Root · 14 generations backK926449 Varian Multileaf Collimator, Release 4.0Varian Assoc., Inc. · 1995
  2. 10 generations between
  3. 3 generations backK171733 TrueBeam, TrueBeam STx, EdgeVarian Medical Systems, Inc. · 2017
  4. 2 generations backK213977 TrueBeam, TrueBeam STx, Edge, VitalBeamVarian Medical Systems, Inc. · 2022
  5. 1 generation backK231317 TrueBeam, TrueBeam STx, Edge, VitalBeamVarian Medical Systems, Inc. · 2023
  6. This deviceK232870 TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1)Varian Medical Systems, Inc. · 2023
  7. Descendant · cites it directly · 0 of its ownK252948 TrueBeam, TrueBeam STX, Edge and VitalBeamVarian Medical Systems, Inc. · 2025
Show all 14 generations
  1. Root · 14 generations backK926449 Varian Multileaf Collimator, Release 4.0Varian Assoc., Inc. · 1995
  2. 13 generations backK973889 Varian Multileaf Collimator with Dynamic Arc Therapy FeatureVarian Medical Systems, Inc. · 1997
  3. 12 generations backK990085 Millennium MLC -120Varian Assoc., Inc. · 1999 · Recalled
  4. 11 generations backK050442 Millennium Multi-Leaf CollimatorVarian Medical Systems · 2005 · Recalled
  5. 10 generations backK071992 High-Definition 120 Multileaf Collimator (HD120 MLC)Varian Medical Systems · 2007 · Recalled
  6. 9 generations backK092871 Trilogy MXVarian Medical Systems, Inc. · 2009 · Recalled
  7. 8 generations backK111106 TruebeamVarian Medical Systems, Inc. · 2011 · Recalled
  8. 7 generations backK123291 TruebeamVarian Medical Systems, Inc. · 2012
  9. 6 generations backK140528 True Beam, True Beam STX, EdgeVarian Medical Systems, Inc. · 2014 · Recalled
  10. 5 generations backK143224 TrueBeam-TrueBeam STx-EdgeVarian Medical Systems, Inc. · 2014 · Recalled
  11. 4 generations backK162472 TrueBeam-TrueBeam STx-EdgeVarian Medical Systems, Inc. · 2017
  12. 3 generations backK171733 TrueBeam, TrueBeam STx, EdgeVarian Medical Systems, Inc. · 2017
  13. 2 generations backK213977 TrueBeam, TrueBeam STx, Edge, VitalBeamVarian Medical Systems, Inc. · 2022
  14. 1 generation backK231317 TrueBeam, TrueBeam STx, Edge, VitalBeamVarian Medical Systems, Inc. · 2023
  15. This deviceK232870 TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1)Varian Medical Systems, Inc. · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K252948TrueBeam, TrueBeam STX, Edge and VitalBeamVarian Medical Systems, Inc. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−14K926449Varian Multileaf Collimator, Release 4.0Varian Assoc., Inc.1995—
−13K973889Varian Multileaf Collimator with Dynamic Arc Therapy FeatureVarian Medical Systems, Inc.1997—
−12K990085Millennium MLC -120Varian Assoc., Inc.19992
−11K050442Millennium Multi-Leaf CollimatorVarian Medical Systems20052
−10K071992High-Definition 120 Multileaf Collimator (HD120 MLC)Varian Medical Systems20074
−9K092871Trilogy MXVarian Medical Systems, Inc.20095
−8K111106TruebeamVarian Medical Systems, Inc.20115
−7K123291TruebeamVarian Medical Systems, Inc.2012—
−6K140528True Beam, True Beam STX, EdgeVarian Medical Systems, Inc.20142
−5K143224TrueBeam-TrueBeam STx-EdgeVarian Medical Systems, Inc.20141
−4K162472TrueBeam-TrueBeam STx-EdgeVarian Medical Systems, Inc.2017—
−3K171733TrueBeam, TrueBeam STx, EdgeVarian Medical Systems, Inc.2017—
−2K213977TrueBeam, TrueBeam STx, Edge, VitalBeamVarian Medical Systems, Inc.2022—
−1K231317TrueBeam, TrueBeam STx, Edge, VitalBeamVarian Medical Systems, Inc.2023—
0 (this device)K232870TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1)Varian Medical Systems, Inc.2023—
+1K252948TrueBeam, TrueBeam STX, Edge and VitalBeamVarian Medical Systems, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199110
199620
199710
199910
200020
200110
200320
200430
200510
200620
200720
200820
201010
201210
201310
201710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K232870, 1995–2025Source: 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 IYE? 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 IYE device

  1. #1 K252977 Halcyon, Ethos Radiotherapy System (5.0)score 18.8 · 18 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
*K231317TrueBeam, TrueBeam STx, Edge, VitalBeam
Summary page 5
…IYE | 21 CFR 892.5050 | Class II PREDICATE DEVICE Predicate Device Name: TrueBeam™ /TrueBeam STx™/Edge™/VitalBeam (K231317) Reference Device(s): No reference devices were used in this submission. DEVICE DESCRIPTION The TrueBeam a…
Varian Medical Systems, Inc.2023—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K252948TrueBeam, TrueBeam STX, Edge and VitalBeamVarian Medical Systems, Inc.20250

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 28 years and passes through 3 companies; a new generation was cleared every 1.7 years on median.
  • 26 of the 39 ancestors have a recall of any class.
  • Of its descendants, K252948 (Varian Medical Systems, Inc., 2025) has gone furthest, with 0 descendants of its own.

How does its category compare?

All IYE devices

IYE Accelerator, Linear, Medical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · IYE

12in 2025

2007: 232008: 142009: 202010: 232011: 112012: 282013: 182014: 202015: 202016: 212017: 232018: 212019: 192020: 202021: 192022: 122023: 182024: 92025: 122026 (partial year): 14
2007high 28 (2012) · low 9 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IYE

170in 2025

2007: 44 days median2008: 69 days median2009: 63 days median2010: 74 days median2011: 94 days median2012: 106 days median2013: 88 days median2014: 100 days median2015: 108 days median2016: 97 days median2017: 94 days median2018: 58 days median2019: 83 days median2020: 67 days median2021: 86 days median2022: 172 days median2023: 129 days median2024: 239 days median2025: 170 days median2026 (partial year): 120 days median
2007high 239 (2024) · low 44 (2007)2026

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

Recalls per year · IYE

1in 2025

2007: 782008: 492009: 222010: 272011: 732012: 202013: 112014: 142015: 82016: 72017: 72018: 72019: 22020: 42021: 52022: 32023: 72024: 12025: 12026 (partial year): 4
2007high 78 (2007) · low 1 (2024)2026

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

Adverse event reports per year · IYE

101in 2025

2007: 1552008: 1142009: 1742010: 2462011: 2802012: 1282013: 962014: 1242015: 1002016: 972017: 1252018: 852019: 912020: 742021: 682022: 662023: 1282024: 812025: 101
2007high 280 (2011) · low 66 (2022)2025

MAUDE reports naming product code IYE, 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
2007234478155
2008146949114
2009206322174
2010237427246
2011119473280
20122810620128
201318881196
20142010014124
2015201088100
20162197797
201723947125
20182158785
20191983291
20202067474
20211986568
202212172366
2023181297128
20249239181
2025121701101
2026141204—

What is it indicated for?

TrueBeam-TrueBeam STx-Edge: The TrueBeamTM, TrueBeam STx and Edge T M Systems are intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body where radiation therapy is indicated for adults and pediatric patients. The TrueBeam radiotherapy system can produce CBCT images that can be used in image guided radiation therapy, and the simulation and planning for adaptive radiation therapy.…

Read the full statement (479 words)

TrueBeam-TrueBeam STx-Edge:

The TrueBeamTM, TrueBeam STx and Edge T M Systems are intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body where radiation therapy is indicated for adults and pediatric patients. The TrueBeam radiotherapy system can produce CBCT images that can be used in image guided radiation therapy, and the simulation and planning for adaptive radiation therapy.

The TrueBeam, TrueBeam STx and Edge Systems may be used in the delivery of radiation for treatment that includes: brain and spine tumors (such as glioma, meningioma, craniopharyngioma, pituitary tumors, spinal cord tumors, hemangioblastoma, orbital tumors, ocular tumors, optic nerve tumors, and skull based tumors), head and neck tumors (such as unknown primary of the head and neck, oral cavity, hypopharynx, larynx, oropharynx, nasopharynx, sinonasal, salivary gland, and thyroid cancer), thoracic tumors (such as lung cancer, esophageal cancer, thymic tumors, and mesothelioma), gynecologic tumors (such as ovarian, cervical, endometrial, vulvar, and vaginal), gastrointestinal tumors (such as gastric, pancreatic, hepatobiliary, colon, rectal, and anal carcinoma), genitourinary tumors (such as prostate, bladder, testicular, and kidney), breast tumors, sarcomas, lymphoid tumors (such as Hodgkin's and non-Hodgkin's lymphoma), skin cancers (such as squamous cell, basal cell, and melanoma), benign diseases (such as schwannoma, arteriovenous malformation, cavernous malformation, trigeminal neuralgia, chordoma, glomus tumors, and hemangiomas), metastasis (including all parts of the body such as brain, bone, liver, lung, kidney, and skin) and pediatric tumors (such as glioma, ependymoma, pituitary tumors, hemangioblastoma, craniopharyngioma, meningioma, metastasis, medulloblastoma, nasopharyngeal tumors, arteriovenous malformation, cavernous malformation, and and skull base tumors), and medically refractory essential tremor (indicated for adults only).

VitalBeam:

VitalBeam@ is intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body where radiation therapy is indicated for adults and pediatric patients.

VitalBeam may be used in the delivery of radiation for treatment that includes: brain and spine tumors (such as glioma, meningioma, craniopharyngioma, pituitary tumors, spinal cord tumors, hemangioblastoma, orbital tumors, ocular tumors, optic nerve tumors, and skull based tumors), head and neck tumors (such as unknown primary of the head and neck, oral cavity, hypopharynx, larynx, oropharynx, nasopharynx, sinonasal, salivary gland, and thyroid cancer), thoracic tumors (such as lung cancer, esophageal cancer, thymic tumors, and mesothelioma), gynecologic tumors (such as ovarian, cervical, endometrial, vulvar, and vaginal), gastrointestinal tumors (such as gastric, pancreatic, hepatobiliary, colon, rectal, and anal carcinoma), genitourinary tumors (such as prostate, bladder, testicular, and kidney), breast tumors, sarcomas, lymphoid tumors (such as Hodgkin's and non-Hodgkin's lymphoma), skin cancers (such as squamous cell, basal cell, and melanoma), benign diseases (such as schwannoma, arteriovenous malformation, cavernous malformation, trigeminal neuralgia, chordoma, glomus tumors, and hemangiomas), metastasis (including all parts of the body such as brain, bone, liver, lung, kidney, and skin) and pediatric tumors (such as glioma, ependymoma, pituitary tumors, hemangioblastoma, craniopharyngioma, meningioma, metastasis, medulloblastoma, nasopharyngeal tumors, arteriovenous malformation, cavernous malformation, and skull base tumors).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K232870: TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K232870

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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