Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Vomed Volzer Medizintechnik GmbH & Co. · 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) |
|---|---|---|---|---|---|
| K023019 | VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000 | Vomed Volzer Medizintechnik GmbH & Co. | 2002-12-10 | 90 | 0 |
| K022257 | VOMED PERIPHERAL VASCULAR ACCESSORIES, MODELS 1010 XXX-7090 | Vomed Volzer Medizintechnik GmbH & Co. | 2002-10-04 | 84 | 0 |
| K022318 | VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES | Vomed Volzer Medizintechnik GmbH & Co. | 2002-09-19 | 73 | 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