VENTURE SOLUTIONS

FDA Device Registration & Listing · Grove City, OH, US · Registration 3030708766

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
3030708766
FEI Number
3030708766
Entity Name
VENTURE SOLUTIONS
City/State/Country
Grove City, OH, US
Establishment Address
3125 LEWIS CENTRE WAY, Grove City, OH 43123, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
VENTURE SOLUTIONS (Owner Number: 10090374)
Owner / Operator Contact Address
1170 GREY FOX RD, Arden Hills, MN 55112, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Specimen Mailer Product InSure One - One Day Fecal Immunochemical Test

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDW Container, Specimen Mailer And Storage, Temperature Controlled, Sterile Pathology Class 1 864.3250 2024-03-19
KHE Reagent, Occult Blood Hematology Class 2 864.6550 2024-03-19

Official Correspondent

Kelley Hardtke

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011945100 VENTURE SOLUTIONS Arden Hills, MN, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K913967 Doxtech, Inc. DOX TAMPERPROOF SPECIMEN CONTAINER SYSTEM 1991-10-18
K162333 Guangzhou Wondfo Biotech Co., Ltd. Wondfo One Step Fecal Occult Blood (FOB) Test 2017-05-14

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2244900 GLOBE SCIENTIFIC, LLC Mahwah, NJ, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030708766. Last updated year: 2026. Please use registration number 3030708766 when referencing this establishment in official correspondence.
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