MEDXL INC
- Type
- Manufacturer
- Location
- Pointe-Claire Quebec, Canada
- Founded
- 2013
- Categories
- Dental Supplies & Equipment, Medical & Healthcare Supplies
Listed in a source registry
Verified facts
- manufacturing-practice-certified (green), checked 2026-08-21 ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- registry-active-global (red), checked 2026-08-12 Corporations Canada (ISED)
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- registry-id-verified (green), checked 2013-11-01 Corporations Canada (ISED)
- registered-since (green), checked 2013-11-01 Corporations Canada (ISED)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)