Data / Medical devices / United States / 3M Company
3M Company: FDA-registered device maker in Aberdeen, SD, United States, 3 510(k) clearances
3M Company is registered with the FDA (registration 1719330) in Aberdeen, SD, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 10, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1719330
- FEI number
- 1000043951
- Address
- 610 North County RD. 19, Aberdeen, SD, United States, 57401
- Owner or operator
- 3M COMPANY (2110898)
- Roles
- Manufacturer
- First device listed
- August 21, 2003
- Registered through
- 2026
- Brand names listed
- 3M, Respirator,surgical, Tape and bandage, adhesive
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mask, Surgical | FXX | 2 | Manufacturer | accessdata.fda.gov |
| Respirator, Surgical | MSH | 2 | Manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 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 |
|---|---|---|---|---|---|---|
| August 10, 2017 | K171116 | 3M VFlex Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S | MSH | Substantially Equivalent | 3M Healthcare | accessdata.fda.gov |
| February 23, 2007 | K063023 | 3M HEALTH CARE PARTICULATE RESPIRATOR AND SURGICAL MASK, MODEL 1870 | MSH | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| 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
- All makers of Tape And Bandage, Adhesive
- All makers of Respirator, Surgical
- All makers of Mask, Surgical
Updated August 10, 2017. 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.