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Data / Medical devices / System, Radiation Therapy, Charged-Particle, Medical

System, Radiation Therapy, Charged-Particle, Medical (LHN): 24 FDA-registered makers in 6 countries

24 establishments in 6 countries are registered with the FDA to make System, Radiation Therapy, Charged-Particle, Medical (product code LHN, Class 2, 21 CFR 892.5050). 19 of them have a 510(k) clearance or PMA approval on file and 5 have a recall event. The FDA has issued 93 510(k) clearances under this code, the latest on September 23, 2026, and lists 53 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
LHN
Device class
2
Regulation
892.5050
Medical specialty
Radiology

Makers by country

CountryMakers
United States13
Germany5
Japan2
Belgium2
India1
France1

Makers of System, Radiation Therapy, Charged-Particle, Medical

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Hitachi High-Tech Corp., KashiwanohaKASHIWA-SHI Chiba, JapanManufacturer11June 11, 2026010api.fda.gov
Mevion Medical Systems, Inc.Littleton, MA, United StatesManufacturer4March 25, 20260100api.fda.gov
Varian Medical Systems Particle Therapy GmbH & Co. KGTroisdorf North Rhine-Westphalia, GermanyManufacturer4April 23, 2026000api.fda.gov
Anzai Medical Co, Ltd.SHINAGAWA-KU Tokyo, JapanComplaint file establishment, Manufacturer3April 5, 2017000api.fda.gov
IBA Dosimetry GmbHSCHWARZENBRUCK Bavaria, GermanyManufacturer2July 17, 2020000api.fda.gov
Ion Beam Applications S.A.LOUVAIN-LA-NEUVE, BE Brabant Wallon, BelgiumManufacturer2August 17, 20170340api.fda.gov
Medcom GMBHDarmstadt Hesse, GermanyManufacturer2September 21, 2018000api.fda.gov
PTW FreiburgFREIBURG Baden-Wurttemberg, GermanyManufacturer2September 10, 1997000api.fda.gov
Ehmet HealthPlymouth, MI, United StatesManufacturer1December 10, 2018000api.fda.gov
Empnia Inc.Eden Prairie, MN, United StatesManufacturer1June 27, 2025000api.fda.gov
Intraop Medical Corp.Fremont, CA, United StatesManufacturer1July 24, 1998010api.fda.gov
Massachusetts General HospitalBoston, MA, United StatesManufacturer1September 27, 2019000api.fda.gov
McLaren Health CareFlint, MI, United StatesManufacturer1February 25, 2016000api.fda.gov
Optivus Proton Therapy, Inc.San Bernardino, CA, United StatesManufacturer1July 21, 2000000api.fda.gov
Orfit Industries NVWIJNEGEM Antwerpen, BelgiumManufacturer1April 8, 2020000api.fda.gov
Pronova Solutions, LLCMaryville, TN, United StatesManufacturer1December 8, 2016000api.fda.gov
Sun Nuclear CorporationMelbourne, FL, United StatesManufacturer1January 25, 2012000api.fda.gov
Varian Medical Systems International India Private LtdPune Maharashtra, IndiaComplaint file establishment, Specification developer1February 21, 2013000api.fda.gov
Varian Medical Systems, IncPalo Alto, CA, United StatesManufacturer1February 21, 2013000api.fda.gov
Anholt Technologies Inc.Avondale, PA, United StatesManufacturer0000api.fda.gov
Brainlab SeMunich Bavaria, GermanyManufacturer0000api.fda.gov
Diacor, Inc.Mount Pleasant, UT, United StatesManufacturer0000api.fda.gov
Dyn'rGARDANNE. Bouches-du-Rhone, FranceManufacturer0000api.fda.gov
Hitachi High-Tech America, Inc. Radiation Therapy DivisionSanta Clara, CA, United StatesContract manufacturer0030api.fda.gov

Updated September 23, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.