Data / Medical devices / Mexico / TE Sensores S. de R.L. de C.V
TE Sensores S. de R.L. de C.V: FDA-registered device maker in Hermosillo Mexico, Mexico, 2 510(k) clearances
TE Sensores S. de R.L. de C.V is registered with the FDA (registration 3030089838) in Hermosillo Mexico, Mexico. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 23, 1992. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030089838
- Address
- Av. Obrero Mundial No. 9 Parque Industrial Dynatech, Colonia el Sahuaro, Hermosillo Mexico, Mexico, 83170
- Owner or operator
- TE Connectivity (10089420)
- Roles
- Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer
- First device listed
- December 6, 2023
- Registered through
- 2026
- Brand names listed
- 19274 T/W PROBE, COBE LAB, 20289 T/W PROBE,SORIN BIO, 21369-16,AIRWAY PROBE,11816-88, 21369-17,AIRWAY PROBE,11817-88, 21664,MEDTR- TP, M957061A001, 21665,MEDTR-ATP210 M939195A002, 21666,MEDTR-1384,M957057A001, Draeger and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Retention Type, Balloon | EZL | 2 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer | accessdata.fda.gov |
| Humidifier, Respiratory Gas, (Direct Patient Interface) | BTT | 2 | Contract manufacturer | accessdata.fda.gov |
| Incubator, Neonatal | FMZ | 2 | Contract 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 |
|---|---|---|---|---|---|---|
| November 23, 1992 | K921561 | YSI MODELS 4400 FOLEY CATHETER TEMPERATURE PROBES | EZL | Substantially Equivalent | Ysis, Inc. | accessdata.fda.gov |
| November 21, 1988 | K883793 | DISPOSABLE TEMPERATURE PROBES (SEVERAL MODELS) | FLL | Substantially Equivalent | Yellow Springs Instrument Co., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Retention Type, Balloon
- All makers of Continuous Measurement Thermometer
- All makers of Incubator, Neonatal
- All makers of Humidifier, Respiratory Gas, (Direct Patient Interface)
Updated November 23, 1992. 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.