Medical device licence · 98723 · Class 2
VIZISHOT 2 FLEX
No longer licensed: cancelled
Licence status Cancelled; first licensed February 28, 2017; ended June 9, 2026. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 98723
- Licence holder
- Gyrus Acmi, IncWestborough, MA, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Single Device
- First licensed
- February 28, 2017
- Ended
- June 9, 2026
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- VIZISHOT 2 FLEX
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 “vizishot”. A notice may cover another product or only some lots: read it to see what it covers.
- ViziShot 2 FlexFebruary 4, 2026 · General and plastic surgery · Labelling and packaging - Performance · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.