Cordis US Corp.

FDA Device Registration & Listing · Santa Clara, CA, US · Registration 3004939290

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
3004939290
FEI Number
3010142363
Entity Name
Cordis US Corp.
City/State/Country
Santa Clara, CA, US
Establishment Address
5452 Betsy Ross Dr, Santa Clara, CA 95054, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Cordis US Corp. (Owner Number: 9056360)
Owner / Operator Contact Address
5452 Betsy Ross Dr, --, Santa Clara, CA 95054, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P040044

All Registered Proprietary Names

Mynx Control Vascular Closure Device MynxGrip Vascular Closure Device MYNX CONTROL™ VENOUS Vascular Closure Device 6F-12F

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MGB Device, Hemostasis, Vascular Unknown Class 3 N/A 2007-12-07

Official Correspondent

Linda Ruedy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cordis US Corp.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1016427 Cordis US Corp. Miami Lakes, FL, US
9616099 Cardinal Health Mexico 244 S de RL de CV Ciudad Juarez Chihuahua, MX

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004939290. Last updated year: 2026. Please use registration number 3004939290 when referencing this establishment in official correspondence.
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