Data / Medical devices / China / Beijing Choice Electronic Technololgy Co., Ltd.
Beijing Choice Electronic Technololgy Co., Ltd.: FDA-registered device maker in Beijing, China, 47 510(k) clearances
Beijing Choice Electronic Technololgy Co., Ltd. is registered with the FDA (registration 3005569927) in Beijing, China. It lists 30 device types. The FDA files 47 510(k) clearances under its listings, the newest dated December 16, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3005569927
- Address
- No.9 Shuangyuan Road, Badachu Hi-tech Zone, Shijingshan District, Beijing, China, 100041
- Owner or operator
- BEIJING CHOICE ELECTRONIC TECHNOLOLGY CO., LTD. (9106400)
- Roles
- Exporter to the US, Foreign private label distributor, Manufacturer, Repackager or relabeler
- First device listed
- August 27, 2008
- Registered through
- 2027
- Brand names listed
- Arm type Blood Pressure Monitor CBP1K1, Arm type Blood Pressure Monitor CBP1K2, Arm type Blood Pressure Monitor CBP1K3, Compressor Nebulizer MDN104, Cooling Gel Patch CCGP1A1, Dental Floss CDF1A1, Dental Floss CDF1A2, Dental Floss CDF1A3 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bottle, Collection, Vacuum | KDQ | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Clinical Electronic Thermometer | SDV | 2 | Manufacturer | accessdata.fda.gov |
| Compressor, Air, Portable | BTI | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Exporter to the US, Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Electrocardiograph | DPS | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Electrode, Cutaneous | GXY | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Exerciser, Non-Measuring | ION | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Floss, Dental | JES | 1 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Generator, Oxygen, Portable | CAW | 2 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Kit, Test, Pregnancy, Hcg, Over The Counter | LCX | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | MWI | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Monitor, Ultrasonic, Fetal | KNG | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Oximeter | DQA | 2 | Exporter to the US, Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Oximeter, Infrared, Sporting, Aviation | OCH | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Oximeter, Wellness | PGJ | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Disposable | IMD | 1 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Reminder, Medication | NXQ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Stimulator, Electrical, Transcutaneous, For Arthritis | NYN | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Exporter to the US, Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Stocking, Elastic | ILG | 1 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Test, Luteinizing Hormone (Lh), Over The Counter | NGE | 1 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Visual, Pregnancy Hcg, Prescription Use | JHI | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 16, 2025 | K252268 | V series portable oxygen concentrator (V5, V5C, V6, V6C) | CAW | Substantially Equivalent | Shenzhen Harveymed Technology Co., Ltd. | accessdata.fda.gov |
| June 21, 2024 | K232975 | Pulse Oximeter (MD300C228) | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| November 30, 2023 | K230587 | Wrist Pulse Oximeter | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| August 12, 2023 | K230172 | Pulse Oximeter | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| March 8, 2023 | K220101 | Pulse Oximeter | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| October 21, 2022 | K221992 | Electronic Pulse Stimulator | NUH | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| March 1, 2022 | K213189 | Wrist-type Fully Automatic Digital Blood Pressure Monitor | DXN | Substantially Equivalent | Joytech Healthcare Co. , Ltd. | accessdata.fda.gov |
| February 11, 2022 | K211400 | Pulse Oximeter | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| January 21, 2022 | K211752 | Infrared Thermometer | FLL | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| November 15, 2021 | K211754 | Vital Signs Monitor | MWI | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| July 12, 2020 | K193627 | Automatic Upper Arm Blood Pressure Monitor | DXN | Substantially Equivalent | Dongguan E-Test Technology Co., Ltd. | accessdata.fda.gov |
| October 11, 2018 | K181503 | Fingertip Pulse Oximeter | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| August 29, 2018 | K181104 | Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style | DXN | Substantially Equivalent | Shenzhen Combei Technology Co., Ltd. | accessdata.fda.gov |
| August 22, 2018 | K173024 | Non-invasive blood pressure measurement systems | DXN | Substantially Equivalent | Joytech Healthcare Co. , Ltd. | accessdata.fda.gov |
| June 18, 2018 | K172895 | AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819 | DXN | Substantially Equivalent | Ageless Health Industrial Co., Ltd. | accessdata.fda.gov |
| January 10, 2018 | K171833 | Digital Blood Pressure Monitor-Wrist Style | DXN | Substantially Equivalent | Shenzhen Combei Technology Co., Ltd. | accessdata.fda.gov |
| April 14, 2017 | K162517 | Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13 | NUH | Substantially Equivalent | Jkh Health Co., Ltd. | accessdata.fda.gov |
| January 9, 2017 | K162083 | RII Multi-function Infrared Thermometer, Model TH52Z | FLL | Substantially Equivalent | Radiant Innovation, Inc. | accessdata.fda.gov |
| November 21, 2016 | K160508 | Electronic Pulse Stimulator | NUH | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| October 5, 2016 | K161560 | Fingertip Pulse Oximeter MD300CN310 | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| August 24, 2016 | K160802 | Infrared Forehead Thermometer, FT-100A | FLL | Substantially Equivalent | Hangzhou Universal Electronic Co., Ltd. | accessdata.fda.gov |
| May 5, 2016 | K153520 | Electronic Pulse Stimulator | NUH | Substantially Equivalent | Jkh Health Co., Ltd. | accessdata.fda.gov |
| April 18, 2016 | K152563 | Pulse Oximeter (MD300M/MD300K2) | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| August 28, 2015 | K151206 | Fingertip Pulse Oximeter | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| April 17, 2015 | K150430 | Arm Blood Pressure Monitor, Wrist Blood Pressure Monitor | DXN | Substantially Equivalent | Fudakang Industrial Co., Ltd. | accessdata.fda.gov |
| January 24, 2014 | K131457 | FETAL ULTRASONIC MONITOR AND ACCESSORIES | KNG | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| November 22, 2013 | K132588 | ADHESIVE ELECTRODES | GXY | Substantially Equivalent | Top-Rank Health Care Equipment Co., Ltd. | accessdata.fda.gov |
| November 15, 2013 | K131921 | ELECTRONIC PULSE STIMULATOR | NUH | Substantially Equivalent | Shenzhen Jingkehui Electronic Co.., Ltd. | accessdata.fda.gov |
| November 12, 2013 | K132085 | ONE STEP HCG TEST STRIP, ONE STEP HCG TEST CASSETTE, ONE STEP HCG TEST MIDSTREAM | LCX | Substantially Equivalent | Co-Innovation Biotech Co., Ltd. | accessdata.fda.gov |
| November 12, 2013 | K131243 | NON-CONTACT INFRARED THERMOMETER | FLL | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| October 16, 2013 | K131047 | FINGERTIP PULSE OXIMETER | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| October 3, 2013 | K130947 | FINGERTIP PULSE OXIMETER | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| August 14, 2013 | K123882 | AGE AUTOMATIC UPPER ARM BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Ageless Health Industrial | accessdata.fda.gov |
| June 19, 2013 | K131395 | TRANSTEK BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Guangdong Transtek Medical Electronics Co., Ltd. | accessdata.fda.gov |
| May 10, 2013 | K123871 | FINGERTIP PULSE OXIMETER | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| August 10, 2012 | K120554 | ARM-TYPE FULLY AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, WRIST-TYPE FULLY AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Sejoy Electronics & Instruments Co., Ltd. | accessdata.fda.gov |
| July 19, 2012 | K112622 | HANDHELD ECG MONITOR | DPS | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| March 30, 2011 | K110721 | GAUNYING INFRARED LAMP | ILY | Substantially Equivalent | Foshan Gaunying Electronics Co., Ltd. | accessdata.fda.gov |
| December 2, 2010 | K101577 | MODIFICATION TO:FINGERTIP PULSE OXIMETER, MODEL MD300C SERIES | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| March 31, 2010 | K093872 | HANDHELD ECG MONITOR, MODEL MD100 | DPS | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| March 4, 2009 | K082487 | M-50 SERIES SPO2 SENSOR | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| January 14, 2008 | K072825 | FINGERTIP PULSE OXIMETER, MODEL MD300I | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| December 18, 2007 | K071930 | ONE STEP HCG URINE PREGNANCY TEST (STRIP), MODEL B01-S, ONE STEP HCG URINE PREGNANCY TEST (CASSETTE) , MODEL B01C | LCX | Substantially Equivalent | Blue Cross Bio-Medical Co., Ltd. | accessdata.fda.gov |
| September 13, 2004 | K041692 | INFRARED EAR THERMOMETER, ET-100 SERIES | FLL | Substantially Equivalent | Hangzhou Hua'An Medical & Health Instruments Co., | accessdata.fda.gov |
| December 10, 2003 | K032720 | GEM-STIM TENS, MODELS GM3XY AND GM3AXY | GZJ | Substantially Equivalent | Gemore Technology Co, Ltd. | accessdata.fda.gov |
| October 7, 2003 | K031413 | VIGORMIST COMPRESSOR NEBULIZER | BTI | Substantially Equivalent | Vega Technologies, Inc. | accessdata.fda.gov |
| May 23, 2001 | K002831 | VEGA ULTRASONIC NEBULIZER | CAF | Substantially Equivalent | Vega Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Oximeter
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Oximeter, Infrared, Sporting, Aviation
- All makers of Continuous Measurement Thermometer
Updated December 16, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.