Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Adeor Medical AG · 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) |
|---|---|---|---|---|---|
| K253772 | Velocity Alpha MR High Speed Surgical Drill System | Adeor Medical AG | 2026-03-06 | 100 | 0 |
| K191479 | Velocity Alpha Highspeed Surgical Drill System | Adeor Medical AG | 2021-04-11 | 677 | 0 |
| K191847 | Adeor Medical nxt Non-stick Bipolar Forceps, Adeor Medical n | Adeor Medical AG | 2020-05-22 | 317 | 0 |
| K130755 | HICUT HIGHSPEED INSTRUMENT | Adeor Medical AG | 2014-06-27 | 465 | 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