Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3018229265

FEI Number

3018229265

Entity Name

LETRONICS, INC.

City/State/Country

Mesquite, TX, US

Establishment Address

2200 Big Town Blvd, Ste 180, Mesquite, TX 75149, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Letronics, Inc. (Owner Number: 10087420)

Owner / Operator Contact Address

2200 Big Town Blvd, Ste 180, Mesquite, TX 75149, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Letronics AnySeat PRM Lift

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSA	Lift, Patient, Non-Ac-Powered	General Hospital	Class 1	880.5510	2024-01-26

Official Correspondent

gregg cohen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Letronics, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0013-2018	Handicare Usa Inc	1	PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018	Handicare AB Maskinvagen	1	Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018229265. Last updated year: 2026. Please use registration number 3018229265 when referencing this establishment in official correspondence.