Data / Medical devices / China / Hangzhou Zeo-Innov Life Technology Co., Ltd.
Hangzhou Zeo-Innov Life Technology Co., Ltd.: FDA-registered device maker in Hangzhou Zhejiang, China, 2 510(k) clearances
Hangzhou Zeo-Innov Life Technology Co., Ltd. is registered with the FDA (registration 3022104448) in Hangzhou Zhejiang, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated May 2, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3022104448
- Address
- R101, building 2, No.291, Fucheng Road, Hangzhou Zhejiang, China, 310018
- Owner or operator
- Hangzhou Zeo-Innov Life Technology Co., Ltd. (10084510)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- March 1, 2022
- Registered through
- 2026
- Brand names listed
- Zeolite Hemostatic Cotton, Zeolite Hemostatic Gauze
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Hemostatic Wound Dressing Without Thrombin Or Other Biologics | QSY | U | 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 |
|---|---|---|---|---|---|---|
| May 2, 2023 | K223495 | Zeolite Hemostatic Cotton | QSY | Substantially Equivalent | Hangzhou Zeo-Innov Life Technology Co., Ltd. | accessdata.fda.gov |
| February 10, 2022 | K211570 | Zeolite Hemostatic Gauze | QSY | Substantially Equivalent | Hangzhou Zeo-Innov Life Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated May 2, 2023. 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.