Data / Medical devices / United States / Venture Solutions
Venture Solutions: FDA-registered device maker in Arden Hills, MN, United States, 1 510(k) clearance
Venture Solutions is registered with the FDA (registration 3011945100) in Arden Hills, MN, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 13, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011945100
- Address
- 1170 Grey Fox RD, Arden Hills, MN, United States, 55112
- Owner or operator
- VENTURE SOLUTIONS (10083973)
- Roles
- Contract manufacturer, Repackager or relabeler
- First device listed
- January 5, 2022
- Registered through
- 2026
- Brand names listed
- InSure One - One Day Fecal Immunochemical Test, Oral Fluid Drugs of Abuse and Alcohol Testing Specimen Collection Device, Specimen Mailer Product, Urine Collection Kit (Excludes Hiv Testing)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Specimen Mailer And Storage, Temperature Controlled, Sterile | KDW | 1 | Contract manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Oral Fluid Drugs Of Abuse And Alcohol Test Specimen Collection Device | PJD | 2 | Repackager or relabeler | accessdata.fda.gov |
| Reagent, Occult Blood | KHE | 2 | Contract manufacturer | accessdata.fda.gov |
| Urine Collection Kit (Excludes Hiv Testing) | OIE | 1 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 13, 1999 | K984361 | ORAL-EZE ORAL FLUID COLLECTION SYSTEM | PJD | Substantially Equivalent | Osborn Laboratories, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Reagent, Occult Blood
- All makers of Urine Collection Kit (Excludes Hiv Testing)
- All makers of Container, Specimen Mailer And Storage, Temperature Controlled, Sterile
- All makers of Oral Fluid Drugs Of Abuse And Alcohol Test Specimen Collection Device
Updated January 13, 1999. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.