STARPLEX SCIENTIFIC CORP.

FDA Device Registration & Listing · Cleveland, TN, US · Registration 3006623380

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
3006623380
FEI Number
3006623380
Entity Name
STARPLEX SCIENTIFIC CORP.
City/State/Country
Cleveland, TN, US
Establishment Address
705 Industrial Drive SW, Cleveland, TN 37311, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Starplex Scientific Corp. (Owner Number: 10024967)
Owner / Operator Contact Address
705 Industrial Drive SW, PO Box 3392, Cleveland, TN 37311, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DisCap; Kangapack; Leakbuster; Pinworm Collector (V302-PIN); Quick Turn; Spout Cap

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NNI Container, Specimen, Non-Sterile Pathology Class 1 864.3250 2008-03-05
FMH Container, Specimen, Sterile Pathology Class 1 864.3250 2008-03-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Starplex Scientific Corp.
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 3006623380. Last updated year: 2026. Please use registration number 3006623380 when referencing this establishment in official correspondence.
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