Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021235837

FEI Number

3021235837

Entity Name

Chongqing Sonmol Technology Co., Ltd.

City/State/Country

Chongqing, CN

Establishment Address

No. 19 Ruihe Road, Shuitu Subdistrict, Liangjiang New Area, Chongqing 400799, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Chongqing Sonmol Technology Co., Ltd. (Owner Number: 10083174)

Owner / Operator Contact Address

No. 19 Ruihe Road, Shuitu Subdistrict, Liangjiang New Area, Chongqing, CN-NOTA 400799, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Nasal Aspirator Nasal Rinse Salt Package, Nasal Irrigator Respiratory Muscle Trainer Peak Flow Meter Peak Flow Meter Handheld steam inhaler Nasal Irrigator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2021-10-31
KAR	Irrigator, Sinus	Ear, Nose, Throat	Class 1	874.4420	2021-10-31
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2021-10-31
BZH	Meter, Peak Flow, Spirometry	Anesthesiology	Class 2	868.1860	2022-01-05
BZH	Meter, Peak Flow, Spirometry	Anesthesiology	Class 2	868.1860	2025-01-08
KFZ	Humidifier, Non-Direct Patient Interface (Home-Use)	Anesthesiology	Class 1	868.5460	2022-08-29
KMA	Irrigator, Powered Nasal	Ear, Nose, Throat	Class 1	874.5550	2021-10-31

Official Correspondent

Yongxu Li

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Chongqing Sonmol Technology 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
K050853	Card Guard Scientific Survival , Ltd.	PMP4 SPIROPRO	2005-05-04
K123945	Monaghan Medical Corp.	STRIVE DUAL ZONE PEAK FLOW METER	2013-04-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021235837. Last updated year: 2026. Please use registration number 3021235837 when referencing this establishment in official correspondence.