ELIXIR MEDICAL CORPORATION

FDA Device Registration & Listing · Milpitas, CA, US · Registration 3005092783

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
3005092783
FEI Number
3005092783
Entity Name
ELIXIR MEDICAL CORPORATION
City/State/Country
Milpitas, CA, US
Establishment Address
920 N. McCarthy Blvd, Suite 100, Milpitas, CA 95035, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
Elixir Medical Corporation (Owner Number: 10027369)
Owner / Operator Contact Address
920 N. McCarthy Blvd, Suite 100, Milpitas, CA 95035, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NIQ Coronary Drug-Eluting Stent Unknown Class 3 N/A 2008-10-30
NIQ Coronary Drug-Eluting Stent Unknown Class 3 N/A 2008-10-30
QMG Shockwave Intravascular Lithotripsy System Unknown Class 3 N/A 2025-02-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Elixir Medical Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005092783. Last updated year: 2026. Please use registration number 3005092783 when referencing this establishment in official correspondence.
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