Data / Medical devices / Canada / Solventum Canada Limited
Solventum Canada Limited: FDA-registered device maker in Morden Manitoba, Canada, 5 510(k) clearances
Solventum Canada Limited is registered with the FDA (registration 3038988287) in Morden Manitoba, Canada. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated February 3, 1998. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3038988287
- Address
- 400 Route 100, Morden Manitoba, Canada, R6M 1Z9
- Owner or operator
- Solventum US LLC (10091183)
- Roles
- Manufacturer
- First device listed
- October 22, 2003
- Registered through
- 2026
- Brand names listed
- 3M Electrosurgical Patient Plate, 3M Electrosurgical Patient Plates, 3M Red Dot Electrodes, 3M Universal Electrosurgical Pad
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Occlusive | NAD | 1 | Manufacturer | accessdata.fda.gov |
| Electrode, Electrocardiograph | DRX | 2 | Manufacturer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | 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 |
|---|---|---|---|---|---|---|
| February 3, 1998 | K974553 | 3M UNIVERSAL ELECTROSURGICAL PAD, SPLIT (9160) 3M UNIVERSAL ELECTROSURGICAL PAD (9130) | GEI | Substantially Equivalent | 3M Healthcare | accessdata.fda.gov |
| January 30, 1998 | K974279 | 3M UNIVERSAL ELECTROSURGICAL PAD, WITH CORD (CATALOG NUMBER 9135), 3M UNIVERSAL ELECTROSURGICAL PAD, SPLIT WITH CORD (C) | GEI | Substantially Equivalent | 3M Healthcare | accessdata.fda.gov |
| February 13, 1990 | K900332 | EM 1149 OPTIMIZE SCOTCHPLATE CONDUC ADHES DISP ELE | GEI | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| November 29, 1983 | K833364 | 3M SCOTCHPLATE II DISPERSIVE ELECTRODE | GEI | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| January 12, 1983 | K823689 | 3M SCOTCHPLATE 51148 SMALL CONDUCTIVE | GEI | Substantially Equivalent | 3M Company | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Stethoscope, Manual
- All makers of Electrode, Electrocardiograph
- All makers of Dressing, Wound, Occlusive
Updated February 3, 1998. 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.