KIT COMPANY

FDA Device Registration & Listing · Phoenix, AZ, US · Registration 3017155466

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
3017155466
FEI Number
3017155466
Entity Name
KIT COMPANY
City/State/Country
Phoenix, AZ, US
Establishment Address
1125 W Pinnacle Peak Rd, Suite 110, Phoenix, AZ 85027, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
The Kit Company, Inc. (Owner Number: 10076550)
Owner / Operator Contact Address
1125 W Pinnacle Peak Rd, Suite 110, Phoenix, AZ 85027, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Kit Company Centrifuge Finger Compressor Blood Specimen Collection Convenience Kit (Excludes HIV) - KIT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2020-07-22
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2021-10-29
PQD Blood Specimen Collection Convenience Kit (Excludes Hiv) Clinical Chemistry Class 2 862.1675 2023-12-18

Official Correspondent

Andres Mola

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Kit Company, 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 3017155466. Last updated year: 2026. Please use registration number 3017155466 when referencing this establishment in official correspondence.
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