Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009383609

FEI Number

3009383609

Entity Name

ORANOXIS INC

City/State/Country

San Diego, CA, US

Establishment Address

7438 Trade Street, San Diego, CA 92121, US

Establishment Type(s)

Manufacture Device in the United States for Export Only,Manufacture Medical Device

Owner / Operator

ORANOXIS INC (Owner Number: 10038851)

Owner / Operator Contact Address

7438 Trade St., San Diego, CA 92121, US

Initial Importer Flag

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
OHQ	Multi-Analyte Controls Unassayed	Clinical Chemistry	Class 1	862.1660	2011-11-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ORANOXIS INC

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 3009383609. Last updated year: 2026. Please use registration number 3009383609 when referencing this establishment in official correspondence.