Data / Medical devices / China / Beijing Choicemmed Technology Co., Ltd.
Beijing Choicemmed Technology Co., Ltd.: FDA-registered device maker in Beijing, China, 6 510(k) clearances
Beijing Choicemmed Technology Co., Ltd. is registered with the FDA (registration 3032013079) in Beijing, China. It lists 9 device types. The FDA files 6 510(k) clearances under its listings, the newest dated December 16, 2025. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3032013079
- Address
- 2nd Floor, Room 201 & 202, No. 2 Building, No. 9 Shuangyuan Road, Shijingshan District, Beijing, China, 100041
- Owner or operator
- Beijing Choicemmed Technology Co., Ltd. (10091759)
- Roles
- Exporter to the US, Repackager or relabeler
- First device listed
- October 30, 2024
- Registered through
- 2027
- Brand names listed
- Insect Bite Relief IBH-001
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Compressor, Air, Portable | BTI | 2 | Exporter to the US | accessdata.fda.gov |
| Generator, Oxygen, Portable | CAW | 2 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | MWI | 2 | Exporter to the US | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Exporter to the US | accessdata.fda.gov |
| Oximeter | DQA | 2 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Oximeter, Infrared, Sporting, Aviation | OCH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Oximeter, Wellness | PGJ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 2 | Exporter to the US | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Exporter to the US, Repackager or relabeler | 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 |
| September 3, 2025 | K250231 | Automatic Upper Arm Blood Pressure Monitor (BA-831X, BA-832X, BA-833X, BA-837X, BA-838X, BA-842X, BA-843X, BA-845X, BA-847X, BA-849X, BA-851X, BA-852X, BA-855X, BA-835, BA-836, BA-839, BA-840, BA-856) | DXN | Substantially Equivalent | Dongguan E-Test Technology Co., Ltd. | accessdata.fda.gov |
| March 8, 2023 | K220101 | Pulse Oximeter | DQA | 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 |
| October 5, 2016 | K161560 | Fingertip Pulse Oximeter MD300CN310 | DQA | Substantially Equivalent | Beijing Choice Electronic Technology Co., Ltd. | accessdata.fda.gov |
| October 7, 2003 | K031413 | VIGORMIST COMPRESSOR NEBULIZER | BTI | Substantially Equivalent | Vega Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Oximeter, Infrared, Sporting, Aviation
- All makers of Compressor, Air, Portable
- All makers of Nebulizer (Direct Patient Interface)
- All makers of Generator, Oxygen, Portable
- All makers of Oximeter
- All makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
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.