Data / Medical devices / China / JWD. Technologies (jiangmen) Co.,ltd.
JWD. Technologies (jiangmen) Co.,ltd.: FDA-registered device maker in Jiangmen Guangdong, China, 4 510(k) clearances
JWD. Technologies (jiangmen) Co.,ltd. is registered with the FDA (registration 3011182134) in Jiangmen Guangdong, China. It lists 12 device types. The FDA files 4 510(k) clearances under its listings, the newest dated September 26, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011182134
- Address
- Block 5 & Block 6, No. 63 Sanjiang Road, Yinzhou Bay Science and Technology Industrial Park Sanjiang, Xinhui, Jiangmen, Guangdong, China, Jiangmen Guangdong, China, 529142
- Owner or operator
- JWD. TECHNOLOGIES (JIANGMEN) CO.,LTD. (10047702)
- Roles
- Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- October 22, 2014
- Registered through
- 2026
- Brand names listed
- Bonus Pacifier Medicine Dispenser, Choking Rescue Device/Anti Choking Device (Model: BSY-001/BSY-002/BSY-003/BSY-004), Clear Way Nasal Aspirator, Digital Thermometer (TH093, TH111, TH074, TH112), Easy Grip Toddler Toothbrush, Medicine Dropper with Spill Guard, Medicine spoon, Safety 1st and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Operating-Room, Wall Vacuum Powered | GCX | 2 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Depressor, Tongue, Non-Surgical | FMA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Oral Administration Set | PXA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Otoscope | ERA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Ring, Teething, Non-Fluid Filled | MEF | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Thermometer, Clinical Mercury | FLK | 2 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| September 26, 2021 | K203731 | DT100 Digital Thermometer | FLL | Substantially Equivalent | Smart Technology Co., Ltd. | accessdata.fda.gov |
| December 16, 2011 | K112289 | DISPOSABLE THERMOMETER COVERS AND SHEATHS | FLL | Substantially Equivalent | Kang ZE Industrial Co. Limited | accessdata.fda.gov |
| August 3, 2010 | K101387 | DIGITAL THERMOMETER, MODELS BT-A11CN, BT-A21CN, BT-A41CN | FLL | Substantially Equivalent | Fudakang Industries Co., Ltd. | accessdata.fda.gov |
| May 23, 1985 | K851146 | DIGITAL THERMOMETER | FLL | Substantially Equivalent | Micro Idea Instrument Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Continuous Measurement Thermometer
- All makers of Otoscope
- All makers of Disinfectant, Medical Devices
- All makers of Apparatus, Suction, Operating-Room, Wall Vacuum Powered
- All makers of Syringe, Irrigating (Non Dental)
Updated September 26, 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.