Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Inter Medical Medizintechnik 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) |
|---|---|---|---|---|---|
| K230393 | UniCam Evo Software | Inter Medical Medizintechnik GmbH | 2023-04-13 | 58 | 0 |
| K132347 | MULTICAM 3000 ECO | Inter Medical Medizintechnik GmbH | 2013-11-20 | 114 | 0 |
| K052473 | CX 250 C PLUS WITH GAMMAXP SOFTWARE, MODEL 0121 0000 | Inter Medical Medizintechnik GmbH | 2005-10-28 | 49 | 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