Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Hasomed GmbH · 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) |
|---|---|---|---|---|---|
| K162683 | RehaStim 2 | Hasomed GmbH | 2017-02-03 | 130 | 0 |
| K132416 | REHASTIM 2, ERIGOPRO (FES) | Hasomed GmbH | 2014-05-28 | 299 | 0 |
| K112844 | REHASTIM 2, REHAMOVE 2 | Hasomed GmbH | 2011-10-27 | 28 | 0 |
| K073237 | REHASTIM & REHAMOVE | Hasomed GmbH | 2007-12-27 | 41 | 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