Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Isodose Control B.V. — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K091145 | FLEXIPLAN 3D AND 3D+ | Isodose Control B.V. | 2009-05-27 | 37 | 0 |
| K082530 | APPLICATORS FOR AFTERLOADING BRACHYTHERAPY | Isodose Control B.V. | 2008-10-30 | 58 | 0 |
| K081112 | FLEXIPLAN BRACHYTHERAPY TREATMENT PLANNING SYSTEM | Isodose Control B.V. | 2008-07-29 | 102 | 0 |
| K070574 | FLEXITRON | Isodose Control B.V. | 2007-04-13 | 44 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda