Solventum US LLC

FDA Device Registration & Listing · Columbia, MO, US · Registration 3036497156

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3036497156
FEI Number
3036497156
Entity Name
Solventum US LLC
City/State/Country
Columbia, MO, US
Establishment Address
5400 Paris Rd, Columbia, MO 65202, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Solventum US LLC (Owner Number: 10091183)
Owner / Operator Contact Address
12930 IH 10 West, San Antonio, TX 78249, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QBP Cap, Device Disinfectant General Hospital Class 2 880.5440 2019-04-01
QBP Cap, Device Disinfectant General Hospital Class 2 880.5440 2019-04-01
QBP Cap, Device Disinfectant General Hospital Class 2 880.5440 2019-04-01
LDE Stethoscope, Manual Cardiovascular Class 1 870.1875 2003-10-22

Official Correspondent

JEFFERY SCHORR

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Solventum US LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004943440 3M Purification, S. de R.L. de C. V. San Luis Potosi Mexico, MX
3003775292 KCI POLYMEDICS BV PEER Limburg, BE
3036108847 Solventum US LLC Eden Prairie, MN, US
3038988287 Solventum Canada Limited Morden Manitoba, CA
3032763783 Solventum Poland Manufacturing SP. ZO.O Wroclaw Dolnoslaskie, PL

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3036497156. Last updated year: 2026. Please use registration number 3036497156 when referencing this establishment in official correspondence.
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