CENTRAL SOLUTIONS, INC.

FDA Device Registration & Listing · KANSAS CITY, KS, US · Registration 1932672

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
1932672
FEI Number
1000138339
Entity Name
CENTRAL SOLUTIONS, INC.
City/State/Country
KANSAS CITY, KS, US
Establishment Address
401 FUNSTON ROAD, KANSAS CITY, KS 66115, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
CENTRAL SOLUTIONS, INC. (Owner Number: 9019377)
Owner / Operator Contact Address
401 FUNSTON ROAD, --, KANSAS CITY, KS 66115, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tri-Cen Whirlpool Disinfectant Pro-Tech Disinfectant Cleaner Pheno-Cen Spray Disinfectant Deodorant Low pH Phenolic 256 Pheno-Cen Detergent Disinfectant 3E-Zyme Triple Enzyme Cleaner CSI Multi-Enzymatic Cleanser

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 1995-06-09
FLG Cleaner, Ultrasonic, Medical Instrument General Hospital Class 1 880.6150 2022-01-26

Official Correspondent

PAUL NOBREGA

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CENTRAL SOLUTIONS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-2025 Young Dental Manufacturing I, LLC 1
BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net contents 16 fl. oz., makes 16 gallons of solution.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1932672. Last updated year: 2026. Please use registration number 1932672 when referencing this establishment in official correspondence.
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