Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009205152

FEI Number

3009205152

Entity Name

SINO MEDICAL SCIENCES TECHNOLOGY INC.

City/State/Country

Tianjin, CN

Establishment Address

TEDA Biopharm Res. Building B and 4th Floor Building A, #5 4th St. TEDA,, Tianjin 300457, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Sino Medical Sciences Technology Inc. (Owner Number: 10062605)

Owner / Operator Contact Address

2nd Floor, Building B, TEDA Biopharm Res, #5, 4th St, TEDA,, Tianjin, CN-TJ 300457, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K223022

PMA Number

N/A

All Registered Proprietary Names

NC ROCKSTAR SC HONKYTONK

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LOX	Catheters, Transluminal Coronary Angioplasty, Percutaneous	Cardiovascular	Class 2	870.5100	2023-01-15
LOX	Catheters, Transluminal Coronary Angioplasty, Percutaneous	Cardiovascular	Class 2	870.5100	2023-02-26

Official Correspondent

Rui WANG

US Agent Details

Eric Cao Business: NOVA VASCULAR Inc. Email: ecao@sinomed.com Phone: (408) 6461320

Related Public Records

Same Entity

Sino Medical Sciences Technology 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-0030-04	N/A	2	Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 2cm Tip 20 mm Balloon, Catalog Number H74902071011
Z-0031-04	N/A	2	Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 2cm Tip 20 mm Balloon, Catalog Number H74902071051
Z-0032-04	N/A	2	Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 1 cm Tip and 20 mm Balloon, Catalog Number H74903628151

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009205152. Last updated year: 2026. Please use registration number 3009205152 when referencing this establishment in official correspondence.