Data / Medical devices / United States / Brevet Inc.
Brevet Inc.: FDA-registered device maker in Huntington Beach, CA, United States, 2 510(k) clearances
Brevet Inc. is registered with the FDA (registration 2025870) in Huntington Beach, CA, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 14, 1989. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2025870
- Address
- 21571 Surveyor Circle, Huntington Beach, CA, United States, 92646
- Owner or operator
- BREVET INC. (10024278)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- June 2, 2008
- Registered through
- 2026
- Brand names listed
- By-pass Syringe- Blood Culture, By-pass Syringe- Luer Access, Syringe, piston
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Percutaneous | DQY | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Contract manufacturer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 14, 1989 | K895753 | BREVET DISPOSABLE CONNECTORS | DQY | Substantially Equivalent | Brevet, Inc. | accessdata.fda.gov |
| July 28, 1988 | K882617 | BREVET CASSETTE STERILIZATION MODULE | FSM | Substantially Equivalent | Brevet, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Tray, Surgical, Instrument
- All makers of Syringe, Piston
- All makers of Catheter, Percutaneous
Updated November 14, 1989. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.