Medical device licence · 77410 · Class 3
TILOOP MESH
No longer licensed: suspended
Licence status Suspended; first licensed June 18, 2008; ended March 27, 2020. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 77410
- Licence holder
- Pfm Medical, Inc.Carlsbad, CA, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Family
- First licensed
- June 18, 2008
- Ended
- March 27, 2020
- Devices covered
- 18
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- TILOOP BRA EXTRALIGHT
- TILOOP BRA LIGHT
- TILOOP CLIP EXTRALIGHT
- TILOOP CLIP LIGHT
- TILOOP FIX LIGHT
- TILOOP FIX STRONG
- TILOOP FOUR EXTRALIGHT
- TILOOP FOUR LIGHT
- TILOOP MESH EXTRALIGHT
- TILOOP MESH LIGHT
- TILOOP PATCH EXTRALIGHT
- TILOOP PATCH LIGHT
- TILOOP TAPE EXTRALIGHT
- TILOOP TAPE LIGHT
- TILOOP TOTAL 4
- TILOOP TOTAL 6
- TILOOP TWO EXTRALIGHT
- TILOOP TWO LIGHT
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 “tiloop”. A notice may cover another product or only some lots: read it to see what it covers.
- TiLoop Mesh (2020-04-10)April 24, 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.