Data / Medical devices / China / Ningbo Verykind Medical Device Co., Ltd.
Ningbo Verykind Medical Device Co., Ltd.: FDA-registered device maker in Ningbo Zhejiang, China, 2 510(k) clearances
Ningbo Verykind Medical Device Co., Ltd. is registered with the FDA (registration 3021604067) in Ningbo Zhejiang, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 30, 2021. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3021604067
- Address
- #100 Jinghua Road, High-tech, Industrial Development Zone Ningbo, 315040 Zhejiang, P.R. China, Ningbo Zhejiang, China, 315040
- Owner or operator
- Ningbo Verykind Medical Device Co., Ltd. (10083880)
- Roles
- Manufacturer
- First device listed
- December 27, 2021
- Registered through
- 2027
- Brand names listed
- David Staplers, Endrive Disposable Powered Endoscopic Linear Cutting Staplers and Cartridges
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Staple, Implantable | GDW | 2 | Manufacturer | accessdata.fda.gov |
| Stapler, Surgical | GAG | 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 |
|---|---|---|---|---|---|---|
| December 30, 2021 | K211458 | Disposable Anorectal Staplers, Disposable Intraluminal Staplers, Disposable Linear Cutting Staplers, Disposable Endoscopic Cutting Staplers | GDW | Substantially Equivalent | Ningbo Verykind Medical Device Co., Ltd. | accessdata.fda.gov |
| May 18, 2021 | K202709 | Disposable Powered Endoscopic Linear Cutting Staplers and Cartridges | GDW | Substantially Equivalent | Ningbo Verykind Medical Device Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 30, 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.