Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO · 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) |
|---|---|---|---|---|---|
| K132102 | BECE CAD ZIRKON HT+ | Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO | 2013-11-12 | 127 | 0 |
| K123929 | BEGOPAL+ | Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO | 2013-03-14 | 84 | 0 |
| K090434 | BECE PRESS | Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO | 2009-07-06 | 137 | 0 |
| K983081 | BEGOPAL 300 | Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO | 1998-10-28 | 56 | 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