Data / Medical devices / Scaler, Ultrasonic / China
FDA-registered makers of Scaler, Ultrasonic in China: 13 establishments
13 establishments in China are registered with the FDA to make Scaler, Ultrasonic (product code ELC). 11 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
- Scaler, Ultrasonic
- Product code
- ELC
- Country
- China
Makers of Scaler, Ultrasonic in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shenzhen Ainengke Electronics Co, Ltd | Shenzhen Guangdong, China | Manufacturer | 3 | December 4, 2000 | 0 | 0 | 0 | api.fda.gov |
| Guilin Woodpecker Medical Instrument Co., Ltd | GUILIN CITY Guangxi, China | Manufacturer | 2 | December 10, 2021 | 0 | 0 | 0 | api.fda.gov |
| Quanzhou Aguru E-Commerce Co., Ltd | Quanzhou Fujian, China | Manufacturer | 2 | July 8, 1993 | 0 | 0 | 0 | api.fda.gov |
| Changzhou Bomedent Medical Technology Co., Ltd | Changzhou Jiangsu, China | Manufacturer | 1 | September 8, 2022 | 0 | 0 | 0 | api.fda.gov |
| Denjoy Dental Co., Ltd | Changsha city Hunan, China | Manufacturer, Repackager or relabeler | 1 | February 13, 2025 | 0 | 0 | 0 | api.fda.gov |
| Foshan Coxo Medical Instrument Co., Ltd. | Foshan Guangdong, China | Manufacturer | 1 | March 23, 2023 | 0 | 0 | 0 | api.fda.gov |
| Guilin Refine Medical Instrument Co., Ltd. | Guilin Guangxi, China | Manufacturer | 1 | November 21, 2023 | 0 | 0 | 0 | api.fda.gov |
| Lakong Medical Devices Co., Ltd. | Dongguan Guangdong, China | Manufacturer | 1 | March 31, 2011 | 0 | 0 | 0 | api.fda.gov |
| Nanning Baolai Medical Instrument Co., Ltd | NANNING Guangxi, China | Manufacturer | 1 | April 6, 2015 | 0 | 0 | 0 | api.fda.gov |
| Nanning VV Dental Co., Ltd. | Nanning Guangxi, China | Manufacturer | 1 | November 21, 2017 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Micro Electric Intelligence Co., Ltd. | Shenzhen Guangdong, China | Exporter to the US, Manufacturer | 1 | July 2, 2024 | 0 | 0 | 0 | api.fda.gov |
| China Zhong Yan Chang Xing International Co. Ltd | Zibo City Shandong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zibo Dante Co, Ltd | Zibo City Shandong, China | Contract manufacturer | 0 | 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.