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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, 1 510(k) clearance

Posey, S. de R.L. de C.V. is registered with the FDA (registration 3031564213) in Tijuana Baja California, Mexico. It lists 24 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 3, 2026.

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Get makers like this oneWatch Posey, S. de R.L. de C.V.
FDA registration number
3031564213
Address
Via Rapida Poniente #16785 Col. Ninos, No. 34 Heroes Este, Tijuana Baja California, Mexico, CP 22120
Owner or operator
TIDI PRODUCTS, LLC (2020362)
Roles
Exporter to the US
First device listed
July 24, 2002
Registered through
2026
Brand names listed
Posey

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Exporter to the USaccessdata.fda.gov
Aid, TransferIKX1Exporter to the USaccessdata.fda.gov
Apron, LeadedEAJ1Exporter to the USaccessdata.fda.gov
Bag, Urine Collection, Leg, For External Use, Non-SterileNNW1Exporter to the USaccessdata.fda.gov
Bed, Ac-Powered Adjustable HospitalFNL2Exporter to the USaccessdata.fda.gov
Cover, Biopsy ForcepsFFF1Exporter to the USaccessdata.fda.gov
Cover, CastKIA1Exporter to the USaccessdata.fda.gov
Device, Fixation, Tracheal TubeCBH1Exporter to the USaccessdata.fda.gov
Device, Intravascular Catheter SecurementKMK1Exporter to the USaccessdata.fda.gov
Drape, Surgical, ExemptPUI2Exporter to the USaccessdata.fda.gov
Fall Prevention Alarm/Sensor Attached OnlyPJP1Exporter to the USaccessdata.fda.gov
Fall Prevention Alarm/Sensor Combination Attached Or UnattachedPJO1Exporter to the USaccessdata.fda.gov
Garment, Protective, For IncontinenceEYQ1Exporter to the USaccessdata.fda.gov
Monitor, Bed PatientKMI1Exporter to the USaccessdata.fda.gov
Orthosis, Limb BraceIQI1Exporter to the USaccessdata.fda.gov
Pad, Neonatal EyeFOK1Exporter to the USaccessdata.fda.gov
Patient Bed With Canopy/RestraintsOYS1Exporter to the USaccessdata.fda.gov
Protector, Skin PressureFMP1Exporter to the USaccessdata.fda.gov
Restraint, ProtectiveFMQ1Exporter to the USaccessdata.fda.gov
Splint, Extremity, Non-Inflatable, External, Non-SterileNOC1Exporter to the USaccessdata.fda.gov
System, Imaging, Pulsed Echo, UltrasonicIYO2Exporter to the USaccessdata.fda.gov
Table And Attachments, Operating-RoomBWN1Exporter to the USaccessdata.fda.gov
Table, Cystometric, ElectricMMZ2Exporter to the USaccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Exporter to the USaccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
September 18, 2009K090773CFI ULTRASOUND PROBE DRAPEIYOSubstantially EquivalentContour Fabricators, Inc.accessdata.fda.gov

Compare with other makers

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.