Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012315039

FEI Number

3012315039

Entity Name

SUZHOU SINNOMED TECHNOLOGIES CO. LTD.

City/State/Country

changshu Jiangsu, CN

Establishment Address

11A, NO.16 Zengfu Road, Baimao, Guli, changshu Jiangsu 215532, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

SINNOMED (Owner Number: 10050100)

Owner / Operator Contact Address

11A, NO.16 Zengfu Road, Baimao, Guli, Changshu, CN-JS 215532, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PILL CRUSHER POUCH

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2021-08-26
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2016-08-30
OHY	Pill Crusher/Cutter	General Hospital	Class 1	880.6430	2015-10-12

Official Correspondent

SONG YANG

US Agent Details

Connie Lewis Email: clewis@maxpertmedical.com Phone: (614) 2045966

Related Public Records

Same Entity

SINNOMED

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
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012315039. Last updated year: 2026. Please use registration number 3012315039 when referencing this establishment in official correspondence.