CLINIQA CORPORATION

FDA Device Registration & Listing · San Marcos, CA, US · Registration 3010725882

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
3010725882
FEI Number
3010725882
Entity Name
CLINIQA CORPORATION
City/State/Country
San Marcos, CA, US
Establishment Address
258 la Moree Rd, San Marcos, CA 92078, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CLINIQA CORPORATION (Owner Number: 2083131)
Owner / Operator Contact Address
495 Enterprise Street, --, San Marcos, CA 92078, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Enzymatic Cleaner Hemoglobin Lyse Reagent Hematology Diluent

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PPM General Purpose Reagent Pathology Class 1 864.4010 2014-01-30
GGK Products, Red-Cell Lysing Products Hematology Class 1 864.8540 2014-01-30
GIF Diluent, Blood Cell Hematology Class 1 864.8200 2014-01-30

Official Correspondent

Dawn Gast

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CLINIQA CORPORATION
View consolidated registration, premarket clearance, and recall records for this applicant.
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Other Registrations for Same Entity

Registration Number Establishment Name Location
2085064 CLINIQA CORPORATION San Marcos, CA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010725882. Last updated year: 2026. Please use registration number 3010725882 when referencing this establishment in official correspondence.
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