Data / Medical devices / United States / Solventum US LLC
Solventum US LLC: FDA-registered device maker in Columbia, MO, United States, 6 510(k) clearances
Solventum US LLC is registered with the FDA (registration 3036497156) in Columbia, MO, United States. It lists 5 device types. The FDA files 6 510(k) clearances under its listings, the newest dated October 29, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036497156
- Address
- 5400 Paris Rd, Columbia, MO, United States, 65202
- Owner or operator
- Solventum US LLC (10091183)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- October 22, 2003
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Liquid | KMF | 1 | Manufacturer | accessdata.fda.gov |
| Cap, Device Disinfectant | QBP | 2 | Manufacturer | accessdata.fda.gov |
| Prism, Fresnel, Ophthalmic | HKT | 1 | Manufacturer | accessdata.fda.gov |
| Stethoscope, Electronic | DQD | 2 | Contract manufacturer | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| October 29, 2020 | K200299 | Curos Jet Disinfecting Cap | QBP | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| August 23, 2016 | K153571 | Cavilon Advanced High Endurance Skin Protectant | KMF | Substantially Equivalent | 3M Healthcare | accessdata.fda.gov |
| December 4, 2014 | K140657 | CUROS RED PORT PROTECTOR | QBP | Substantially Equivalent | Ivera Medical, Inc. | accessdata.fda.gov |
| November 26, 2012 | K121171 | CUROS TIP | QBP | Substantially Equivalent | Ivera Medical, Inc. | accessdata.fda.gov |
| January 12, 2012 | K111992 | CUROS PORT PROTECTOR | QBP | Substantially Equivalent | Ivera Medical, Inc. | accessdata.fda.gov |
| February 5, 1996 | K955103 | 3M NO STING BARRIER FILM | KMF | Substantially Equivalent | 3M Medical Products Group | accessdata.fda.gov |
Compare with other makers
- All makers of Cap, Device Disinfectant
- All makers of Stethoscope, Electronic
- All makers of Bandage, Liquid
- All makers of Prism, Fresnel, Ophthalmic
- All makers of Stethoscope, Manual
Updated October 29, 2020. 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.