Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Bud Industries, Inc. — 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) |
|---|---|---|---|---|---|
| K912521 | DENTAL IMPLANT SYSTEM 4.0MM AND 5.5MM LENGTH | Bud Industries, Inc. | 1995-05-02 | 1440 | 0 |
| K913688 | BUD MAXILLOFACIAL IMPLANT SYSTEM | Bud Industries, Inc. | 1992-05-05 | 260 | 0 |
| K902331 | BUD DENTAL IMPLANT SYSTEM | Bud Industries, Inc. | 1991-07-05 | 407 | 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