PLASTIKON HEALTHCARE

FDA Device Registration & Listing · Lawrence, KS, US · Registration 3009840089

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
3009840089
FEI Number
3009840089
Entity Name
PLASTIKON HEALTHCARE
City/State/Country
Lawrence, KS, US
Establishment Address
3780 Greenway Cir, Lawrence, KS 66046, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Plastikon Healthcare (Owner Number: 10042054)
Owner / Operator Contact Address
3780 Greenway Circle, Lawrence, KS 66046, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Prompt Inoculation System-D

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LIE Reagent/Device, Inoculum Calibration Microbiology Class 2 866.1640 2023-09-30

Official Correspondent

Sandy Dixon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Plastikon Healthcare
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3008229479 PlasTAT Limited Dongguan City Guangdong, CN
3009974297 Plastikon Industries Hayward, CA, US
3010392593 Inplast Plastic & Electronics Co., Ltd Suzhou New District Jiangsu, CN

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009840089. Last updated year: 2026. Please use registration number 3009840089 when referencing this establishment in official correspondence.
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