Data / Medical devices / Mexico / Medtronic Mexico Eg
Medtronic Mexico Eg: FDA-registered device maker in EMPALME Sonora, Mexico, 2 PMA approvals
Medtronic Mexico Eg is registered with the FDA (registration 3004497303) in EMPALME Sonora, Mexico. It lists 1 device type. The FDA files 2 PMA approvals under its listings, the newest dated April 1, 2011. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3004497303
- Address
- Carretera Intl. KM. 1969 Guadalajara-Nogales KM.2, EMPALME Sonora, Mexico, 85340
- Owner or operator
- Medtronic, Inc. (2112641)
- Roles
- Manufacturer
- First device listed
- December 22, 2010
- Registered through
- 2027
- Brand names listed
- Endurant II AUI Stent Graft System, Endurant II Stent Graft System, Endurant IIs Stent Graft System, Endurant Stent Graft System, Talent Occluder with Occluder Delivery System, Valiant Thoracic Stent Graft System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Endovascular Graft, Aortic Aneurysm Treatment | MIH | 3 | Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| April 1, 2011 | P100040 | VALIANT THORACIC STENT GRAFT SYSTEM | MIH | 69 | February 27, 2026 | accessdata.fda.gov |
| December 16, 2010 | P100021 | MEDTRONIC VASCULAR ENDURANT STENT GRAFT SYSTEM | MIH | 129 | May 12, 2026 | accessdata.fda.gov |
Compare with other makers
Updated February 27, 2026. 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.