Cardiva Medical, Inc.

FDA Device Registration & Listing · Santa Clara, CA, US · Registration 3015145497

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015145497
FEI Number
3015145497
Entity Name
Cardiva Medical, Inc.
City/State/Country
Santa Clara, CA, US
Establishment Address
1615 Wyatt Drive, Santa Clara, CA 95054, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
CARDIVA MEDICAL, INC. (Owner Number: 9058841)
Owner / Operator Contact Address
1615 Wyatt Dr, Santa Clara, CA 95054, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P120016

All Registered Proprietary Names

VASCADE MVP VVCS 6-12F VASCADE MVP XL VVCS VASCADE 5F VCS VASCADE 6/7F VCS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MGB Device, Hemostasis, Vascular Unknown Class 3 N/A 2013-04-15

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CARDIVA MEDICAL, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011469355 Cardiva Medical, Inc. Guaymas Sonora, MX

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015145497. Last updated year: 2026. Please use registration number 3015145497 when referencing this establishment in official correspondence.
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