Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Brevet, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 23, 1991: SMALL INSTRUMENT STERILIZATION/BUR BOX.
| Date | Record | Source |
|---|---|---|
| May 23, 1991 | SMALL INSTRUMENT STERILIZATION/BUR BOXK910794 · EJL | 510(k) clearances |
| Dec 4, 1989 | BREVET FLOSS PICK (AUTOCLAVE STERILIZER)K895958 · EKJ | 510(k) clearances |
| Nov 29, 1989 | BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)K895959 · EKJ | 510(k) clearances |
| Nov 14, 1989 | BREVET DISPOSABLE CONNECTORSK895753 · DQY | 510(k) clearances |
| Oct 5, 1988 | BREVET DENTAL INSTRUMENTSK883126 · EKJ | 510(k) clearances |
| Jul 28, 1988 | BREVET CASSETTE STERILIZATION MODULEK882617 · FSM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
