Data / Medical devices / China / Ningbo Dearevery Electrical Technology Co., Ltd.
Ningbo Dearevery Electrical Technology Co., Ltd.: FDA-registered device maker in Yuyao Zhejiang, China, 1 510(k) clearance
Ningbo Dearevery Electrical Technology Co., Ltd. is registered with the FDA (registration 3016915446) in Yuyao Zhejiang, China. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 6, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016915446
- Address
- Building 6, No. 18, East Section of North Outer Ring Road, Simen Town, Yuyao Zhejiang, China, 315470
- Owner or operator
- Ningbo Dearevery Electrical Technology CO., LTD. (10090959)
- Roles
- Manufacturer
- First device listed
- June 7, 2024
- Registered through
- 2026
- Brand names listed
- BY-R202,BY-R203,BY-R204,BY-R205,BY-R206,BY-R207,BY-R208,BY-R301,BY-R302,BY-R303,BY-R304, Bath Chair:XY-Y101,XY-Y102,XY-Y103,XY-Y104,XY-Y105,XY-Y106,XY-Y107,XY-Y108, Bathroom Rail:WH-T101,WH-T102,WH-T103,WH-T104,WH-T105,WH-T106,WH-T107,WH-T108,WH-T201, Bedside Rail:CH-T101,CH-T102,CH-T103,CH-T104,CH-T105,CH-T106,CH-T107,CH-T108,CH-T201, Breast Pump (D-111), CH-T202,CH-T203,CH-T204,CH-T205,CH-T206,CH-T207,CH-T208,CH-T209,CH-T210,CH-T211,CH-T212, Cold Therapy Device: CT-P701, CT-P702, CT-R711, Infrared Lamp: RT-T601, RT-T602, RT-T603, RT-T604, RT-T605 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Attachment, Commode, Wheelchair | INB | 1 | Manufacturer | accessdata.fda.gov |
| Bed, Manual | FNJ | 1 | Manufacturer | accessdata.fda.gov |
| Chair And Table, Medical | KMN | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Adjustable, Mechanical | INN | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Water Circulating | ILO | 2 | Manufacturer | accessdata.fda.gov |
| Pump, Breast, Non-Powered | HGY | 1 | Manufacturer | accessdata.fda.gov |
| Pump, Breast, Powered | HGX | 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 |
|---|---|---|---|---|---|---|
| June 6, 2024 | K232774 | Wearable Breast Pump,Model S18 | HGX | Substantially Equivalent | Ningbo Dearevery Electronic Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Bed, Manual
- All makers of Chair And Table, Medical
- All makers of Pump, Breast, Non-Powered
- All makers of Attachment, Commode, Wheelchair
- All makers of Pack, Hot Or Cold, Water Circulating
- All makers of Chair, Adjustable, Mechanical
Updated June 6, 2024. 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.