Data / Medical devices / China / Prodol Meditec Limited
Prodol Meditec Limited: FDA-registered device maker in Zhuhai Guangdong, China, 1 510(k) clearance
Prodol Meditec Limited is registered with the FDA (registration 3007817051) in Zhuhai Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 21, 2012. Registered through 2026. 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
- 3007817051
- Address
- 1/F, 4/F, Block C, NO. 18, 7th Science Ave., Zhuhai Guangdong, China, 519085
- Owner or operator
- PRODOL MEDITEC S.A. (9079460)
- Roles
- Manufacturer
- First device listed
- November 9, 2005
- Registered through
- 2026
- Brand names listed
- Airtraq A-360 WiFi Camera (A-360), Airtraq A-390 WiFi Camera Accessories (A-390-ACC), Airtraq A-390 WiWi Camera (A-390), Airtraq A-390 Wifi Camera Full KIT (A-390-KIT), Airtraq Avant Demo Optics (A-581), Airtraq Avant Docking station (A-590), Airtraq Avant Optics (A-501), Airtraq Avant Regular Blade (A-511) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laryngoscope, Rigid | CCW | 1 | 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 |
|---|---|---|---|---|---|---|
| June 21, 2012 | K121378 | AIRTRAQ SP AIRTRAQ AVANT | CCW | Substantially Equivalent | Prodol Meditec , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 21, 2012. 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.