Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
VBM 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) |
|---|---|---|---|---|---|
| K200190 | ScalpelCric | VBM Medizintechnik GmbH | 2020-10-30 | 277 | 0 |
| K112783 | MANUJET III | VBM Medizintechnik GmbH | 2011-12-22 | 87 | 0 |
| K955461 | TRANSTRACHEAL CATHETER (ACC. RAVUSSIN). | VBM Medizintechnik GmbH | 1997-03-19 | 476 | 3 |
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