Data / Medical devices / China / Deepintec Scientific Co., Ltd
Deepintec Scientific Co., Ltd: FDA-registered device maker in Beijing, China, 4 510(k) clearances
Deepintec Scientific Co., Ltd is registered with the FDA (registration 3026317086) in Beijing, China. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 19, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3026317086
- Address
- Building No. 4, 18Kechuang 10th Street, DBA, Beijing, Beijing, China, 100176
- Owner or operator
- Deepintec Scientific Co., Ltd (10093943)
- Roles
- Manufacturer
- First device listed
- August 15, 2025
- Registered through
- 2026
- Brand names listed
- 14" Willow Guidewire, Willow 14 Guidewire, Willow 18 Guidewire, Willow 24 Guidewire
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Guide, Wire, Catheter, Neurovasculature | MOF | 2 | Manufacturer | accessdata.fda.gov |
| Wire, Guide, Catheter | DQX | 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 |
|---|---|---|---|---|---|---|
| March 19, 2026 | K260537 | Willow 24 Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
| February 13, 2026 | K260130 | Willow 18 Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
| November 26, 2025 | K253168 | 0.014 Willow Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
| July 17, 2025 | K243756 | 0.014 Willow Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
Compare with other makers
Updated March 19, 2026. 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.