Data / Medical devices / Mexico / 3M Edumex, S.A De C.V
3M Edumex, S.A De C.V: FDA-registered device maker in CD. JUAREZ Chihuahua, Mexico, 1 510(k) clearance
3M Edumex, S.A De C.V is registered with the FDA (registration 9680284) in CD. JUAREZ Chihuahua, Mexico. It lists 28 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 4, 1991. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9680284
- FEI number
- 3002809016
- Address
- Avenida Ramon Rivera Lara 6620 Parque Industrial Ramon Rivera Lara, CD. JUAREZ Chihuahua, Mexico, 32605
- Owner or operator
- 3M COMPANY (2110898)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- December 15, 1992
- Registered through
- 2026
- Brand names listed
- 3M, 3M Surgical Masks, 3M Tie-On Surgical Mask, 3M, BAG, INTESTINE, BANDAGE, ELASTIC, BEDDING, DISPOSABLE, MEDICAL, BINDER, ABDOMINAL and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| March 4, 1991 | K910182 | 3M BRAND EAR LOOP FACE MASK, 2000F | FXX | Substantially Equivalent | 3M Company | accessdata.fda.gov |
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Updated March 4, 1991. 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.