Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Miha Bodytec GmbH · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K221498 | Miha Bodytec II | Miha Bodytec GmbH | 2022-10-07 | 137 | 0 |
| K201975 | miha bodytec II | Miha Bodytec GmbH | 2021-03-11 | 238 | 0 |
| K182519 | Miha Bodytec II | Miha Bodytec GmbH | 2019-06-07 | 267 | 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