Data / Medical devices / China / Cemho Medical Technology (Guangdong) Co., Ltd.
Cemho Medical Technology (Guangdong) Co., Ltd.: FDA-registered device maker in Meizhou Guangdong, China, 1 510(k) clearance
Cemho Medical Technology (Guangdong) Co., Ltd. is registered with the FDA (registration 3021355406) in Meizhou Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 16, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3021355406
- Address
- Cemho Medical Industrial Park West of Xinghe Line, Dongguan Shijie (Xingning) Industrial Transfer Industrial Park, Xingning, Meizhou Guangdong, China, 514500
- Owner or operator
- Cemho Medical Technology (Guangdong) Co., Ltd. (10083604)
- Roles
- Manufacturer
- First device listed
- December 5, 2021
- Registered through
- 2027
- Brand names listed
- Automatic Blood Pressure Monitor, CH-S691L,CH-B607,CH-B606,CH-S692L,CH-S602,CH-W701L,CH-S693L,CH-B601L,CP-B01,CH-S603, CZ-B201,CZ-B202,CZ-B203,CZ-B205,CZ-B206,CZ-B207,CZ-B208,CZ-B209, CZ-B501,CZ-B505,CZ-B506,CZ-B507,CZ-B511,CZ-B512,CZ-B513,CZ-B515, CZ-B701, CZ-B702, CZ-B703, CZ-B705, CZ-B706,CZ-B707, CZ-B708, CZ-B709, CZ-B710, CZ-B711, CZ-B712, CZ-B713, CZ-B715, CZ-B716,CZ-B717,CZ-B718,CZ-B719,CZ-B720,CZ-B721,CZ-B722,CZ-B723,CZ-B725,CZ-B726,CZ-B727,CZ-B728,CZ-B729,CZ-B730,CZ-B732, CZ-B733,CZ-B735,CZ-B736,CZ-B737,CZ-B738,CZ-B739,CZ-B750,CZ-B751,CZ-B752,CZ-B753,CZ-B755,CZ-B756,CZ-B757,CZ-B758,CZ-B801, CZ-B802,CZ-B803,CZ-B805,CZ-B807,CZ-B808,CZ-B809,CZ-B810, Cervical Spine Massager: CH-140, CH-141, CH-142, CH-143 CH-144, CH-145, CH-146, CH-147, CH-148, CH-149; and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter | QUG | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | 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 |
|---|---|---|---|---|---|---|
| July 16, 2025 | K251102 | Automatic Blood Pressure Monitor (CH-S691L, CH-B607, CH-B606, CH-S692L, CH-S602, CH-W701L, CH-S693L, CH-B601L, CP-B01, CH-S603) | DXN | Substantially Equivalent | Cemho Medical Technology (Guangdong) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Massager, Therapeutic, Electric
- All makers of Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter
Updated July 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.