Data / Medical devices / China / Conmo Electronic Company Limited
Conmo Electronic Company Limited: FDA-registered device maker in Huizhou City Guangdong, China, 3 510(k) clearances
Conmo Electronic Company Limited is registered with the FDA (registration 3010968402) in Huizhou City Guangdong, China. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated February 25, 2021. Registered through 2027. FDA data exported November 3, 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
- 3010968402
- Address
- Conmo Intelligent Valley Industrial Park, No. 463, Longshan 4th Road Daya Bay West Area Street, Daya Bay District, Huizhou City Guangdong, China, 516083
- Owner or operator
- CONMO ELECTRONIC COMPANY LIMITED (10046996)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- June 11, 2014
- Registered through
- 2027
- Brand names listed
- 5255180, 55814072F, 558140733F, 55834102F, 57374072F, 57714192F, 577141933F, 578941033FW, 57924072F, 5320104, 578040733FW, 57934072F, 5329324, BCA-381BC/BCA-382BC, BM100-EN, Body Composition Analyzer, Body Fat Analyzer and Scale, DPT-IFT100 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Body Composition | MNW | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Analyzer, Body Composition, Exempt | PUH | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| February 25, 2021 | K202420 | Infrared Forehead Thermometer | FLL | Substantially Equivalent | Conmo Electronic Company Limited | accessdata.fda.gov |
| December 30, 2020 | K202372 | Upper Arm Electronic Blood Pressure Monitor | DXN | Substantially Equivalent | Conmo Electronic Company Limited | accessdata.fda.gov |
| May 30, 2014 | K140594 | BODY FAT ANALYZER AND SCALE | MNW | Substantially Equivalent | Conmo Electronic Company Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Continuous Measurement Thermometer
- All makers of Analyzer, Body Composition
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Analyzer, Body Composition, Exempt
Updated February 25, 2021. 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.