Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Brevet, Inc. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
54 daysmedian FDA review time
87 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K910794 | SMALL INSTRUMENT STERILIZATION/BUR BOX | Brevet, Inc. | 1991-05-23 | 87 | 0 |
| K895958 | BREVET FLOSS PICK (AUTOCLAVE STERILIZER) | Brevet, Inc. | 1989-12-04 | 54 | 0 |
| K895959 | BREVET FLOSS PICK (COLD STERILIZATION FLUIDS) | Brevet, Inc. | 1989-11-29 | 49 | 0 |
| K895753 | BREVET DISPOSABLE CONNECTORS | Brevet, Inc. | 1989-11-14 | 49 | 0 |
| K883126 | BREVET DENTAL INSTRUMENTS | Brevet, Inc. | 1988-10-05 | 71 | 0 |
| K882617 | BREVET CASSETTE STERILIZATION MODULE | Brevet, Inc. | 1988-07-28 | 34 | 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