Medical device licence · 90207 · Class 3
REGENEREX PATELLAS
No longer licensed: cancelled
Licence status Cancelled; first licensed November 29, 2012; ended July 28, 2017. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 90207
- Licence holder
- Biomet Orthopedics, Ata Biomet Sports Medicine, Ata Biomet Biologics, Ata Biomet TraumaWarsaw, IN, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Family
- First licensed
- November 29, 2012
- Ended
- July 28, 2017
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- REGENEREX PRIMARY PATELLA
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 “regenerex”. A notice may cover another product or only some lots: read it to see what it covers.
- REGENEREX PRIMARY TAPER (2020-09-11)September 25, 2020 · Medical devices · Medical devices · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.