Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in BelgiumLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Ion Beam Applications and its 1 subsidiaries with 42 device recalls and 17 510(k) clearances. The most recent is a device recall dated Apr 1, 2025: myQA iON; Article Number: MQ10-000;.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Ion Beam Applications and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Apr 1, 2025 | myQA iON; Article Number: MQ10-000;Class II · Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a sp | Device recalls |
| Jul 17, 2020 | myQA iONK201798 · LHN | 510(k) clearances |
| Jan 23, 2020 | Blue Phantom PTK191821 · LHN | 510(k) clearances |
| Aug 17, 2017 | IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class)K163500 · LHN | 510(k) clearances |
| Aug 9, 2016 | Proton Therapy System - Proteus 235 (Proteus One, Proteus Plus, Proteus TK2)K152224 · LHN | 510(k) clearances |
| Jul 10, 2014 | GANTRY BEAM LINEK132919 · LHN | 510(k) clearances |
| Nov 20, 2013 | I2CK132847 · LHN | 510(k) clearances |
| Aug 6, 2010 | MODIFICATION TO IBA PROTON THERAPY SYSTEM-PROTEUS 235K101508 · LHN | 510(k) clearances |
| Jul 21, 2010 | IBA PROTON THERAPY SYSTEM, MODEL PROTEUS 235K100766 · LHN | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
