Solventum US, LLC is one of 16094 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solventum US, LLC - FDA 510(k) Cleared Devices
Recent clearances: 3M™ Attest™ Steam Chemical Integrator (1243A, 1243B, 1243RE, 1243RES), Tegaderm Post-Op Transparent Antimicrobial Dressing
2
Total
2
Cleared
0
Denied
Solventum US, LLC has 2 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Latest FDA clearance: Sep 2026. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Solventum US, LLC Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Solventum US, LLC
2 devices