Data / Medical devices / United States / Solutions, Inc.
Solutions, Inc.: FDA-registered device maker in Jeffersonville, IN, United States, 1 510(k) clearance
Solutions, Inc. is registered with the FDA (registration 3004055392) in Jeffersonville, IN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 10, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004055392
- Address
- 6213 Gheens Mill Rd, Jeffersonville, IN, United States, 47130
- Owner or operator
- SOLUTIONS, INC. (9059037)
- Roles
- Specification developer
- First device listed
- March 30, 2006
- Registered through
- 2026
- Brand names listed
- Sharps Away Reusable Containers
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| July 10, 1995 | K943765 | SHARPS AWAY | FMI | Substantially Equivalent | Biomedical Waste Systems, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 10, 1995. 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.