Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007483335

FEI Number

3007483335

Entity Name

Qingdao Leckie Foam Products Co. Ltd.

City/State/Country

Qingdao Shandong, CN

Establishment Address

Rm. 101, No.2, Building 8 Fen He Road, Qingdao E. & T. D. Z., Qingdao Shandong 266555, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Leckie Medical Products, Inc. (Owner Number: 10023739)

Owner / Operator Contact Address

1212 E El Dorado Street, West Covina, CA 91790, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Danny Ties Tracheostomy Ties

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBH	Device, Fixation, Tracheal Tube	Anesthesiology	Class 1	868.5770	2007-12-12

Official Correspondent

James Leckie

US Agent Details

James Leckie Business: Leckie Medical Products, Inc. Email: jlleckie@earthlink.net Phone: (626) 4886262

Related Public Records

Same Entity

Leckie Medical Products, Inc.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007483335. Last updated year: 2026. Please use registration number 3007483335 when referencing this establishment in official correspondence.