NINGBO KK-BIOSCIENCE CO., LTD.

FDA Device Registration & Listing · Ningbo Zhejiang, CN · Registration 3018269548

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3018269548
FEI Number
3018269548
Entity Name
NINGBO KK-BIOSCIENCE CO., LTD.
City/State/Country
Ningbo Zhejiang, CN
Establishment Address
No.38, Dongzhou Industrial Park, Xi`dian, Ninghai, Ningbo Zhejiang 315613, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Ningbo KK-Bioscience Co., Ltd. (Owner Number: 10080171)
Owner / Operator Contact Address
No.38, Dongzhou Industrial Park, Xi`dian, Ninghai, Ningbo, CN-ZJ 315613, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Portable DVT System Deep vein thrombosis (DVT) sleeve massage sleeve Compression Garments Pressure Infusion Bag Cold and Compression Therapy Auto chill cold therapy device

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2026-02-11
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2023-07-29
KZD Infusor, Pressure, For I.V. Bags General Hospital Class 1 880.5420 2021-01-17
ILO Pack, Hot Or Cold, Water Circulating Physical Medicine Class 2 890.5720 2025-12-09
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2022-12-13

Official Correspondent

Abby Liu

US Agent Details

Fanny Zhao Business: J & F Technology Service Email: info@jf-yiliao.com Phone: (909) 5100201

Related Public Records

Same Entity

Ningbo KK-Bioscience 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
K170216 Tactile Systems Technology, Inc. (Dba Tactile Medical) Flexitouch System 2017-05-26
K100306 Covidien KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES 2010-05-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018269548. Last updated year: 2026. Please use registration number 3018269548 when referencing this establishment in official correspondence.
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