Data / Medical devices / China / Wat Medical Technology Inc.
Wat Medical Technology Inc.: FDA-registered device maker in Ningbo Zhejiang, China, 5 510(k) clearances
Wat Medical Technology Inc. is registered with the FDA (registration 3014649088) in Ningbo Zhejiang, China. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated February 26, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014649088
- Address
- Room 703, 705, 707,No.2 North Taoyuan Road, Ningbo Zhejiang, China, 315600
- Owner or operator
- WAT Medical Technology Inc. (10058335)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- August 27, 2018
- Registered through
- 2026
- Brand names listed
- ELECTRODE, HeadaTerm2 Electrodes, TENS Device-EmeTerm 2, Model: YF-ZTY-E2, TENS Device-HeadaTerm, EEspress, TENS device-EmeTerm, TENS device-HeadaTerm 2 (Model: YF-HT2)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Electrical, Transcutaneous, For Migraine | PCC | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer | accessdata.fda.gov |
| Tester, Electrode/Lead, Electroencephalograph | GYA | 1 | 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 26, 2024 | K230782 | TENS device-HeadaTerm 2 (Model: YF-HT2) | PCC | Substantially Equivalent | Wat Medical Technology, Inc. | accessdata.fda.gov |
| April 23, 2022 | K220503 | TENS device-EmeTerm 2, Model: YF-ZTY-E2 | GZJ | Substantially Equivalent | Wat Medical Technology, Inc. | accessdata.fda.gov |
| September 13, 2018 | K172450 | TENS device-HeadaTerm, eEspress | PCC | Substantially Equivalent | Wat Medical Technology (Ningbo) Co., Ltd. | accessdata.fda.gov |
| April 19, 2018 | K172478 | TENS device-EmeTerm, CinvStop | GZJ | Substantially Equivalent | Wat Medical Technology (Ningbo) Co., Ltd. | accessdata.fda.gov |
| November 22, 2013 | K132588 | ADHESIVE ELECTRODES | GXY | Substantially Equivalent | Top-Rank Health Care Equipment Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Tester, Electrode/Lead, Electroencephalograph
- All makers of Electrode, Cutaneous
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Stimulator, Nerve, Electrical, Transcutaneous, For Migraine
Updated February 26, 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.