Posey S. de R.L. de C.V.

FDA Device Registration & Listing · Tijuana, Baja California Mexico, MX · Registration 3029906632

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3029906632
FEI Number
3029906632
Entity Name
Posey S. de R.L. de C.V.
City/State/Country
Tijuana, Baja California Mexico, MX
Establishment Address
Blvd. Encino Norte Numero 10001, Colonia Fideicomiso El Florido,, Tijuana, Baja California Mexico 22245, MX
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TIDI PRODUCTS, LLC (Owner Number: 9921057)
Owner / Operator Contact Address
570 Enterprise Dr, Neenah, WI 54956, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQM Camera, Surgical And Accessories General, Plastic Surgery Class 1 878.4160 1992-07-16
MMZ Table, Cystometric, Electric Gastroenterology, Urology Class 2 876.4890 2019-01-22
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2019-01-22
FFF Cover, Biopsy Forceps Gastroenterology, Urology Class 1 876.1075 2021-11-08
PUI Drape, Surgical, Exempt General, Plastic Surgery Class 2 878.4370 2019-01-22

Official Correspondent

Kelsey Weiland

US Agent Details

Amanda Altan Business: TIDI PRODUCTS, LLC Email: aaltan@tidiproducts.com Phone: (218) 5914542

Related Public Records

Same Entity

TIDI PRODUCTS, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3002563411 POSEY, S. de R.L. de C.V. TIJUANA Baja California, MX
3042176500 Posey, S. De R.L. De C.V. Tijuana Baja California, MX
2182318 TIDI PRODUCTS, LLC NEENAH, WI, US
3010699203 Posey, S. de R.L. de C.V. Tijuana Baja California, MX
3031564213 Posey, S. de R.L. de C.V. Tijuana Baja California, MX

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K882805 Coopervision-Cilco CILCO VILLASENOR PACHYMETER 1988-08-12
K791040 Shimadzu Corp. SECTOR SCANNER, SDU-100, COMPUTERIZED 1979-10-04
K162372 Qt Ultrasound, LLC QT Ultrasound Breast Scanner-1 2017-06-06
K930964 Acuson Corp. ACUSON MODEL #29001 (DIAGNOSTIC ULTRASOUND DEVICE) 1994-10-26
K052355 U-Systems, Inc. AUTOMATED BREAST ULTRASOUND SYSTEM, MODEL ABUS 2005-09-14

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-2011 Verathon, Inc. 2
BVI 9600 Bladder Volume Instrument, Aorta Scan Mode The BladderScan BVI 9600 with AortaScan Mode is a user-selectable, dual-function ultrasound device that projects ultrasound energy either into the lower abdomen to obtain an image of the bladder for measuring bladder volume, or into the mid-abdomen to obtain an image of the abdominal aorta for aortic diameter measurements.
Z-0004-2011 Verathon, Inc. 2
AortaScan AMI 9700 The AortaScan AMI 9700 is an ultrasound device that projects ultrasound energy into the mid-abdomen to obtain an image of the abdominal aorta for aortic diameter measurements
Z-0005-2011 Verathon, Inc. 2
BladderScan BVM 9500 The BladderScan BVM 9500 is intended to project ultrasound energy through the lower abdomen to obtain an image of the bladder and measure urinary bladder volume and mass noninvasively.
Z-0027-2014 SonoSite, Inc. 2
P21x/5-1 MHz transducer, Part Number P07698-23 Product Usage: The P21x/5-1 MHz phased array transducer is designed for cardiac, abdominal and obstetric, TCD and orbital exams. It supports 2D with SonoMB Multi Beam Technology and Auto Gain capabilities, SonoHD Imaging Technology, Tissue Harmonic Imaging, M-Mode, Velocity Color Flow Doppler, Color Power Doppler (CDP), Pulsed Wave (PW), TDI Pulsed Wave, and Continuous Wave Doppler.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029906632. Last updated year: 2026. Please use registration number 3029906632 when referencing this establishment in official correspondence.
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