Data / Medical devices / Activator, Ultraviolet, For Polymerization / China
FDA-registered makers of Activator, Ultraviolet, For Polymerization in China: 6 establishments
6 establishments in China are registered with the FDA to make Activator, Ultraviolet, For Polymerization (product code EBZ). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. 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.
- Device
- Activator, Ultraviolet, For Polymerization
- Product code
- EBZ
- Country
- China
Makers of Activator, Ultraviolet, For Polymerization in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Foshan Coxo Medical Instrument Co., Ltd. | Foshan Guangdong, China | Manufacturer | 2 | April 11, 2025 | 0 | 0 | 0 | api.fda.gov |
| Changzhou Sifary Medical Technology Co., Ltd. | Changzhou Jiangsu, China | Manufacturer | 1 | November 23, 2022 | 0 | 0 | 0 | api.fda.gov |
| Foshan CICADA Dental Instrument Co., Ltd. | Foshan Guangdong, China | Manufacturer | 1 | February 13, 2020 | 0 | 0 | 0 | api.fda.gov |
| Guilin Refine Medical Instrument Co., Ltd. | Guilin Guangxi, China | Manufacturer | 1 | November 15, 2023 | 0 | 0 | 0 | api.fda.gov |
| Guilin Woodpecker Medical Instrument Co., Ltd | GUILIN CITY Guangxi, China | Manufacturer | 1 | March 19, 2008 | 0 | 0 | 0 | api.fda.gov |
| Premium Plus (dongguan) Limited | Dongguan Guangdong, China | Manufacturer | 1 | April 10, 2025 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.