Data / Medical devices / United States / 3M Company
3M Company: FDA-registered device maker in Valley, NE, United States, 1 510(k) clearance
3M Company is registered with the FDA (registration 1929938) in Valley, NE, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 1, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1929938
- Address
- 600 East Meigs ST., Valley, NE, United States, 68064
- Owner or operator
- 3M COMPANY (2110898)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- December 6, 2007
- Registered through
- 2026
- Brand names listed
- Electrosurgical, cutting & coagulation & accessories
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Contract manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | 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 |
|---|---|---|---|---|---|---|
| May 1, 1996 | K955382 | 3M MODEL 1860 HEALTH CARE PARTICULATE RESPIRATOR TYPE N95 | FXX | Substantially Equivalent | 3M Company | accessdata.fda.gov |
Compare with other makers
Updated May 1, 1996. 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.