Data / Medical devices / Mexico / IVEMSA S.A. de C.V DIVISION AG INDUSTRIES
IVEMSA S.A. de C.V DIVISION AG INDUSTRIES: FDA-registered device maker in Tijuana Baja California, Mexico, 1 510(k) clearance
IVEMSA S.A. de C.V DIVISION AG INDUSTRIES is registered with the FDA (registration 3015134079) in Tijuana Baja California, Mexico. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 14, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015134079
- Address
- Andador vecinal 11902, Interior L2-A Colonia Carretera Tijuana- Tecate, Tijuana Baja California, Mexico, 22253
- Owner or operator
- AG Industries (9041666)
- Roles
- Manufacturer
- First device listed
- January 19, 2006
- Registered through
- 2026
- Brand names listed
- AG Circuit, breathing (w connector, adaptor, y piece), AG Disinfectant, medical devices, AG FIBER, MEDICAL, ABSORBENT, AG FLOWMETER, CALIBRATION, GAS, AG Filter, bacterial, breathing-circuit, AG Flowmeter, tube, thorpe, back-pressure compensated, AG Protector, skin pressure, AG STRAP, HEAD, GAS MASK and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Manufacturer | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Manufacturer | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Manufacturer | accessdata.fda.gov |
| Filter, Bacterial, Breathing-Circuit | CAH | 2 | Manufacturer | accessdata.fda.gov |
| Flowmeter, Calibration, Gas | BXY | 1 | Manufacturer | accessdata.fda.gov |
| Flowmeter, Tube, Thorpe, Back-Pressure Compensated | CAX | 1 | Manufacturer | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Manufacturer | accessdata.fda.gov |
| Strap, Head, Gas Mask | BTK | 1 | Manufacturer | accessdata.fda.gov |
| Tubing/Tubing With Filter, Insufflation, Laparoscopic | NKC | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Filter, Membrane | JRL | 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 |
|---|---|---|---|---|---|---|
| December 14, 2005 | K052087 | BREATHING FILTER BACTERIAL/VIRAL, MODEL AG7178 | CAH | Substantially Equivalent | Ag Industries | accessdata.fda.gov |
Compare with other makers
- All makers of Flowmeter, Calibration, Gas
- All makers of Disinfectant, Medical Devices
- All makers of Filter, Bacterial, Breathing-Circuit
- All makers of Strap, Head, Gas Mask
- All makers of Protector, Skin Pressure
- All makers of Tubing/Tubing With Filter, Insufflation, Laparoscopic
Updated December 14, 2005. 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.