Data / Medical devices / United States / Prevent Plus, LLC.
Prevent Plus, LLC.: FDA-registered device maker in Saint Louis, MO, United States, 1 510(k) clearance
Prevent Plus, LLC. is registered with the FDA (registration 3012669304) in Saint Louis, MO, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 25, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012669304
- Address
- 4220 Duncan Ave Suite 201, Saint Louis, MO, United States, 63110
- Owner or operator
- Prevent-Plus, LLC (10052036)
- Roles
- Specification developer
- First device listed
- June 3, 2016
- Registered through
- 2026
- Brand names listed
- Preventogen
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Liquid | KMF | 1 | 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 |
|---|---|---|---|---|---|---|
| June 25, 2004 | K032948 | ELASTIC SKIN LIQUID BANDAGE | KMF | Unknown | Medpak, LLC | accessdata.fda.gov |
Compare with other makers
Updated June 25, 2004. 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.