Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031564213

FEI Number

3031564213

Entity Name

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

City/State/Country

Tijuana Baja California, MX

Establishment Address

Via Rapida Poniente #16785 Col. Ninos, No. 34, Heroes Este, Tijuana Baja California CP 22120, MX

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

TIDI PRODUCTS, LLC (Owner Number: 2020362)

Owner / Operator Contact Address

570 Enterprise Dr, Neenah, WI 54956, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Posey

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NOC	Splint, Extremity, Non-Inflatable, External, Non-Sterile	General, Plastic Surgery	Class 1	878.3910	2011-12-28
FOK	Pad, Neonatal Eye	General Hospital	Class 1	880.5270	2006-11-13
OYS	Patient Bed With Canopy/Restraints	General Hospital	Class 1	880.6760	2021-12-21
PJP	Fall Prevention Alarm/Sensor Attached Only	General Hospital	Class 1	880.2400	2015-04-30
BWN	Table And Attachments, Operating-Room	General, Plastic Surgery	Class 1	878.4950	2011-12-28
MMZ	Table, Cystometric, Electric	Gastroenterology, Urology	Class 2	876.4890	2025-11-25
PJO	Fall Prevention Alarm/Sensor Combination Attached Or Unattached	General Hospital	Class 1	880.2400	2015-04-30
FMP	Protector, Skin Pressure	General Hospital	Class 1	880.6450	2005-04-29
IKX	Aid, Transfer	Physical Medicine	Class 1	890.5050	2005-04-29
IQI	Orthosis, Limb Brace	Physical Medicine	Class 1	890.3475	2005-08-17
LYU	Accessory, Surgical Apparel	General, Plastic Surgery	Class 1	878.4040	2018-10-24
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2006-05-10
FMQ	Restraint, Protective	General Hospital	Class 1	880.6760	2010-02-26
EAJ	Apron, Leaded	Radiology	Class 1	892.6500	2024-10-22
KIA	Cover, Cast	General Hospital	Class 1	880.6185	2022-12-08
NNW	Bag, Urine Collection, Leg, For External Use, Non-Sterile	Gastroenterology, Urology	Class 1	876.5250	2012-11-18
KMI	Monitor, Bed Patient	General Hospital	Class 1	880.2400	2006-05-16

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
3029906632	Posey S. de R.L. de C.V.	Tijuana, Baja California Mexico, MX
2182318	TIDI PRODUCTS, LLC	NEENAH, WI, US
3010699203	Posey, S. de R.L. de C.V.	Tijuana Baja California, MX

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K812396	Northwest Surgical Concepts, Inc.	ARTHRO-PREP REST	1981-11-20
K962327	Sekure Seat Corp.	SEKURE SEAT ADULT PASSIVE RESTRAINING DEVICE	1997-03-06
K963243	Heelbo, Inc.	HEELBO BLAZER SLEEVED JACKET	1996-10-01

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3043047582	OY PRIMO FINLAND AB	Vaasa Pohjanmaa, FI
3018759542	DIMENSION ORTHO Inc.	Philadelphia, PA, US
3009605026	JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD.	Yancheng Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031564213. Last updated year: 2026. Please use registration number 3031564213 when referencing this establishment in official correspondence.