Data / Medical devices / Mexico / Posey S. de R.L. de C.V.
Posey S. de R.L. de C.V.: FDA-registered device maker in Tijuana, Baja California Mexico, Mexico, 1 510(k) clearance
Posey S. de R.L. de C.V. is registered with the FDA (registration 3029906632) in Tijuana, Baja California Mexico, Mexico. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 18, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3029906632
- Address
- Blvd. Encino Norte Numero 10001 Colonia Fideicomiso El Florido, Tijuana, Baja California Mexico, Mexico, 22245
- Owner or operator
- TIDI PRODUCTS, LLC (9921057)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- July 16, 1992
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Camera, Surgical And Accessories | KQM | 1 | Manufacturer | accessdata.fda.gov |
| Cover, Biopsy Forceps | FFF | 1 | Contract manufacturer | accessdata.fda.gov |
| Drape, Surgical, Exempt | PUI | 2 | Manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | Manufacturer | accessdata.fda.gov |
| Table, Cystometric, Electric | MMZ | 2 | 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 |
|---|---|---|---|---|---|---|
| September 18, 2009 | K090773 | CFI ULTRASOUND PROBE DRAPE | IYO | Substantially Equivalent | Contour Fabricators, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Imaging, Pulsed Echo, Ultrasonic
- All makers of Drape, Surgical, Exempt
- All makers of Table, Cystometric, Electric
- All makers of Camera, Surgical And Accessories
- All makers of Cover, Biopsy Forceps
Updated September 18, 2009. 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.