Clariance, Sas
Clariance, Sas holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2021, with 1 FDA device recall on record.
Top product codes for Clariance, Sas
FDA recalls by Clariance, Sas
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Clariance, Sas
- K202032 — Idys LLIF 3DTi
- K202956 — Erisma LP Navigated Instruments
- K200920 — Idys ALIF ZP 3DTi
- K192168 — Idys ALIF ZP 3DTi
- K191263 — Idys ALIF TiVac
- K183259 — Idys TLIF TiVac
- K172465 — Idys TLIF 3DTi Cages
- K172083 — Idys ALIF System
- K170163 — Erisma® LP Spinal Fixation System
- K162367 — Erisma® LP MIS
- K153326 — Erisma-LP Spinal Fixation System
Data sourced from openFDA. This site is unofficial and independent of the FDA.