Ethos Treatment Management

Catalogue number 3.0, listed by Varian Medical Systems, Inc, United States, under System, Planning, Radiation Therapy Treatment. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
33510(k) clearances naming this product code
25recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Fujian (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MUJ
Manufacturer City Province Registered as Device types
Philips Healthcare (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Manteia Technologies Co., Ltd. Xiamen Fujian Manufacturer 3
Masep Medical Science & Technology DEVELOPMENT(SHENZHEN)Co. Shenzhen Guangdong Manufacturer 2
Suzhou Linatech Medical Science AND Technology Co., Ltd. Suzhou Jiangsu Manufacturer 2
Varian Medical Systems China Co., Ltd. Beijing Beijing Manufacturer 2

Record

Regulatory record for Ethos Treatment Management
Listed by Varian Medical Systems, Inc, United States
FDA product code MUJ
Device type System, Planning, Radiation Therapy Treatment
Device class Class 2
Regulation 21 CFR 892.5050
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K232923
Record published 2024-05-10

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Ethos Treatment Management
Catalogue number Size Status
3.0 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
RayStation RaySearch Laboratories AB (publ) 29
System, Planning, Radiation Therapy Treatment Nucletron B.V. 17
Panther TPS Prowess, Inc. 14
RayCare RaySearch Laboratories AB (publ) 12
Accuray Precision® Treatment Planning System Accuray Incorporated 7
Monaco Elekta Inc. 7
Eclipse Treatment Planning System for External Beam Radiation Therapy Varian Medical Systems, Inc 6
syngo.via RT Image Suite Siemens Healthcare Limited 5
Eclipse Treatment Planning System Varian Medical Systems, Inc 5
Corvus 09 Best Nomos 4
Monaco Elekta Solutions AB 4
XKnife® Integra Lifesciences Corporation 4

Showing 12 of 98. All products under System, Planning, Radiation Therapy Treatment

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K260750 2026-07-08
K252304 2026-03-18
K242463 2024-12-13
K242378 2024-12-11
K241876 2024-10-23
K232400 2023-09-08
K230557 2023-05-26
K211881 2021-09-02
K203469 2021-04-19
K203766 2021-02-12
K201607 2020-07-10
K200608 2020-04-03
K181145 2018-05-18
K172163 2017-08-15
K170969 2017-07-05
K152393 2015-09-18
K141248 2014-09-05
K141283 2014-08-07
K133247 2014-02-07
K133331 2014-01-27
K131891 2013-09-25
K102011 2010-09-03
K091492 2009-06-18
K073020 2007-12-19
K071760 2007-11-09
K071873 2007-08-09
K050296 2005-11-03
K051497 2005-07-18
K041403 2004-07-26
K021268 2002-05-22
K012017 2001-07-12
K002312 2000-08-30
K984532 1999-08-09

Recalls

8 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2018-12-26 Class II Software design There is an anomaly with the Eclipse(TM) Treatment Planning System [TPS] Proton Convolution Superposition [PCS] dose calculation algorithm. The PCS algo- rithm calculates the water equivalent range incorrectly for non-square 3D CT images ( 1450 devices 2021-03-10
2016-01-11 Class II Software design When using PBC 11.0.31 to calculate the dose for a conventional arc field with more than 100 segments for Eclipse versions 11.0, 13.0, 13.5 or 13.6, the displayed dose does not correspond to the calculated Monitor Units (MU). Potential for 9499 2017-10-25
2015-09-28 Class II Software design (manufacturing process) An anomaly was identified with the ARIA for Radiation Oncology software with a Clinical Assessment license. Admin Instructions may not print on drug order prescriptions or be transmitted with e-Rx. 1971 units 2017-05-12
2014-08-18 Class II Software design Due to user error, the 4DITC can improperly allow users to clear a safety interlock imposed by the 4DITC on behalf of Varian’s Bar Code Conical Verification system from the BrainLab’s ExacTract console when it is used with BCCV. 512 affected devices 2015-07-30
2013-11-18 Class II Software design An anomaly has been traced to a software deficiency within the Plan Parameters workspace. When a dose relevant parameter is changed and “do no clear MUs and Reference Point dose” is selected, the Monitor units may change. 6701 2015-03-13
2013-01-28 Class II Software design The calculation of dose dynamic plans containing different energy fields is incorrect when the Pencil Beam Convolution 11.0 algorithm (PBC 11.0) is used. 1168 units 2014-04-04
2012-08-17 Class II Software design Varian has identified an anomaly with the Eclipse Treatment Planning where an outdated assigned Hounsfield Unit [HU] value can be used for dose calculation when the clock on the Eclipse Client Workstation is not synchronized with the Databa 6087 2014-08-06
2012-06-18 Class II Software design (manufacturing process) Varian has identified an anomaly with the Eclipse Treatment Planning (for radiotherapy treatments) where changing the prescription in a calculated VMAT or RapidArc plan may lead to Monitor Units which do not reflect the new prescription. If 7113 units 2014-08-06
2012-01-30 Not classified Device Design Varian has been identified an anomaly with the Eclipse Treatment Planning System where the calculated dose distribution is not updated or invalidated when a recalculation or reload is performed while the compensator or fluence editor is ope 12,077 units ***AMENDED TO 13,527 units*** 2014-08-15
2011-12-12 Not classified Software design An anomaly has been identified with the Eclipse Treatment Planning System when planning for the Siemens Multileaf Collimator (MLC) where a virtual jaw can be positioned inside the MLC aperture and then used as the beam limiting device for t 11807 units, ***12-12-12 Amended to: 13, 616 units*** 2014-08-15
2011-10-31 Not classified Device Design An anomaly has been identified with Varian Eclipse and RT Chart where adding a reference point
in RT Chart and editing the field dose contributions may change the Prescribed Dose Per Fraction
in Eclipse.
2014-06-06
2011-07-07 Not classified Software design An anomaly has been identified in the 4D Structure Merge option of certain versions of Varian’s Eclipse Treatment Planning System. The treatment field energy may change from the current selection to a previous selection without user interve 2014-04-04
2011-06-30 Not classified Software design In affected Eclipse versions, the treatment field energy may change from the current selection to a previous selection without use intervention and without invalidating the MU or calculated dose distribution. 2436 2014-05-09
2011-05-20 Not classified Software design A software anomaly has been identified with the Eclipse Monte Carlo (eMC) algorithm where not-equidistant data points in the open beam profile used during configuration may lead to inaccurate results. 10,356 2012-07-13
2011-05-13 Not classified Software design In affected Eclipse versions, user editing of the MLC Leaf positions may not automatically invalidate calculated dose distributions. 10,097***12-12-12 AMENDED TO: 10664 units*** 2014-08-15
2011-05-03 Not classified Software design In affected Analytical Anisotropy Algorithm versions when modeling the second source, the collimator jaw positions are read from the first control point of the field. This can cause the delivered dose to be higher than planned locally by up 5201 units ***12-12-12 AMENDED TO: 5448 units*** 2014-07-09
2011-04-04 Not classified Software design An anomaly in Eclipse Treatment Planning System, versions 8.0 to 8.6, whereby Actual SSD (source surface distance) value may not correspond to the Planned SSD value after Planning Approval. 5288 units 2012-06-27
2010-08-11 Not classified Software design Medical device for brachytherapy treatment may cause users to enter incorrect syntax and lead to potential misinterpretation of patient treatment plan. 1252 units 2011-11-25
2010-05-13 Not classified Software design Incorrect treatment plan or record: A software design deficiency has the potential for corrupted treatment plan records or treatment records in cases where multiple users editing a record simultaneously can result in a corrupted (but access 2417 units***12-20-12 AMENDED TO: 49 units*** 2012-02-24
2009-12-09 Not classified Software design Potential for misdelivery of treatment– When preparing a treatment plan involving a split, the device may calculate excessive or insufficient monitor units for the treatment plan. 3177 unit 2012-02-24
2009-07-17 Not classified Software design Software Issue/Mistreatment Potential– Due to software issues, dose distribution may be incorrect and unintended radiation doses may be delivered. 1 2010-11-27
2008-10-02 Not classified Software design When using the multiple static segment option, the device may alter dose delivery. 64 units 2010-11-27
2008-02-13 Not classified Software design A software error causes the wedge accessory calculation to be ignored in the radiotherapy treatment plan. 90 units 2011-05-17
2004-06-24 Not classified Other a malfunction in the software of the VARiS versions 6.2.27 and 6.2.35 which is used to set up radiation therapy devices which will reset parameters to null for future treatments if a patient receives treatment on a non-varian machine and a 28 units 2004-12-23
0010-08-17 Not classified Software design Possible incorrect dose calculation: An anomaly in certain Eclipse versions where, under certain specific sequences of user actions, the dose distribution may fail to be re-calculated even though changes have been made which affect dose. 7019 2011-07-21

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer