Medical device licence · 96284 · Class 3
FEBRIDX
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed December 22, 2015; ended December 9, 2025. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 96284
- Licence holder
- Lumos Diagnostics IncorporatedCarlsbad, CA, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Test Kit
- First licensed
- December 22, 2015
- Ended
- December 9, 2025
- Devices covered
- 3
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- FEBRIDX
- FEBRIDX NEGATIVE CONTROL
- FEBRIDX POSITIVE CONTROL
Recalls and safety alerts that mention it
Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “febridx”. A notice may cover another product or only some lots: read it to see what it covers.
- FebriDx (2020-12-21)December 31, 2020 · Medical devices · COVID - Medical devices · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.