Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011244061

FEI Number

3011244061

Entity Name

SHENZHEN KINGOD SILICONE RUBBER PRODUCTS CO.,LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

1F and 2F, No. 20, Shijing Road, Fumin Community, Fucheng Street,, Longhua District, Shenzhen Guangdong 518109, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Shenzhen Kingod Silicone Rubber Products Co.,Ltd (Owner Number: 10047587)

Owner / Operator Contact Address

1F and 2F, No. 20, Shijing Road, Fumin Community, Fucheng Street,, Longhua District,, Shenzhen City, CN-GD 518109, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Saliva Ejector Mouthpiece

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DYN	Mouthpiece, Saliva Ejector	Dental	Class 1	872.6640	2014-10-08

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Shenzhen Kingod Silicone Rubber Products Co.,Ltd

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K781592	Henry Schein, Inc.	SURGICAL ASPIRATOR TIPS	1978-12-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011244061. Last updated year: 2026. Please use registration number 3011244061 when referencing this establishment in official correspondence.