Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Storz Medical AG · 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) |
|---|---|---|---|---|---|
| K203710 | Storz Medical MAGNETOLITH Muscle Stimulator | Storz Medical AG | 2021-05-03 | 133 | 0 |
| K202112 | Storz Medical Duolith SD1 T-Top & Tower System with C-Actor | Storz Medical AG | 2021-02-21 | 206 | 0 |
| K173692 | D-Actor 200 Vibration Massage System | Storz Medical AG | 2018-04-13 | 133 | 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