Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010262192

FEI Number

3010262192

Entity Name

ADC NINGBO CO., LTD.

City/State/Country

Ningbo Zhejiang, CN

Establishment Address

Suite # 1406, #181, Zhongshan East Road, Ningbo Zhejiang 315000, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

ADC Ningbo Co., Ltd. (Owner Number: 10046012)

Owner / Operator Contact Address

Suite # 1406, #181, Zhongshan East Road, Ningbo, CN-ZJ 315000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ADC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2014-01-23
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2014-01-23
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2014-01-23
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	2015-04-09
DXN	System, Measurement, Blood-Pressure, Non-Invasive	Cardiovascular	Class 2	870.1130	2015-11-18
DQD	Stethoscope, Electronic	Cardiovascular	Class 2	870.1875	2019-04-21
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2014-01-23
GWX	Fork, Tuning	Neurology	Class 1	882.1525	2025-12-07
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2015-02-05
FLL	Continuous Measurement Thermometer	General Hospital	Class 2	880.2910	2015-11-18
BZS	Stethoscope Head	Anesthesiology	Class 1	868.1930	2014-01-23
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2014-01-23
CAE	Airway, Oropharyngeal, Anesthesiology	Anesthesiology	Class 1	868.5110	2014-05-19

Official Correspondent

Jackie Wu

US Agent Details

Marc Blitstein Email: mblitstein@adctoday.com Phone: (631) 2739600

Related Public Records

Same Entity

ADC Ningbo 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
K831001	Frontier Products	UNICUFF-BLOOD PRESSURE CUFF	1983-07-28
K253089	Shenzhen Best Electronics Co., Ltd.	NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)	2026-02-13
K972301	Rudolf Riester GmbH & Co. KG	BIG BEN SQUARE, BIG BEN ROUND	1997-09-17
K100940	Andon Health Co, Ltd.	FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-5965	2010-06-29
K251581	Shenzhen Hingmed Medical Instrument Co., Ltd.	Wearable Ambulatory Blood Pressure Monitor (WBP-02A)	2026-02-13

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0032-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Z-0033-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.
Z-0034-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.
Z-0002-2014	King Systems Corp.	1	King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

Similar Registrations

Registration Number	Establishment Name	Location
3031192529	Zhejiang LuDe Technology Development Co., Ltd.	Wenzhou Zhejiang, CN
3002865611	BALLERSTEDT GMBH	Reinbek Schleswig-Holstein, DE
3009154535	WENZHOU KANGSHUN MEDICAL DEVICES CO.,LTD.	Wenzhou City Zhejiang, CN
1058002	Technicuff Corp.	LEESBURG, FL, US
3001570235	GE Medical Systems Information Technologies, Inc.	Waukesha, WI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010262192. Last updated year: 2026. Please use registration number 3010262192 when referencing this establishment in official correspondence.