Data / Medical devices / United States / Cardiva Medical, Inc.
Cardiva Medical, Inc.: FDA-registered device maker in Santa Clara, CA, United States, 1 PMA approval
Cardiva Medical, Inc. is registered with the FDA (registration 3015145497) in Santa Clara, CA, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated January 31, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015145497
- Address
- 1615 Wyatt Drive, Santa Clara, CA, United States, 95054
- Owner or operator
- CARDIVA MEDICAL, INC. (9058841)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- April 15, 2013
- Registered through
- 2026
- Brand names listed
- VASCADE 5F VCS, VASCADE 6/7F VCS, VASCADE MVP VVCS 6-12F, VASCADE MVP XL VVCS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Hemostasis, Vascular | MGB | 3 | Complaint file establishment, Specification developer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| January 31, 2013 | P120016 | VASCADE VASCULAR CLOSURE SYSTEM | MGB | 40 | September 10, 2026 | accessdata.fda.gov |
Compare with other makers
Updated September 10, 2026. 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.