Clariance is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clariance - FDA 510(k) Cleared Devices
Recent clearances: Elegance® Anterior Cervical plate, Idys® LIF, Erisma® Lp Spinal Fixation System
10
Total
10
Cleared
0
Denied
Clariance has 10 FDA 510(k) cleared orthopedic devices. Based in Cumming, US.
Latest FDA clearance: Jan 2025. Active since 2012.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and Clariance, Inc..
FDA 510(k) Regulatory Record - Clariance
10 devices
Cleared
Jan 14, 2025
Elegance® Anterior Cervical plate
Orthopedic
26d
Cleared
Dec 31, 2024
Idys® LIF
Orthopedic
34d
Cleared
Jul 24, 2024
Erisma® Lp Spinal Fixation System
Orthopedic
27d
Cleared
Apr 26, 2024
Erisma® Deformity Spinal System
Orthopedic
28d
Cleared
Mar 22, 2024
Idys® C ZP 3DTi
Orthopedic
7d
Cleared
Mar 30, 2022
Aggeris™-C
Orthopedic
68d
Cleared
Apr 12, 2021
Idys ALIF 3DTi
Orthopedic
371d
Cleared
Nov 13, 2013
IDYS(TM) C
Orthopedic
230d
Cleared
Oct 10, 2013
IDYS LIF CAGES
Orthopedic
168d
Cleared
Aug 13, 2012
ERISMA-LP
Orthopedic
179d