Optos Plc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Optos Plc. has 15 FDA 510(k) cleared ophthalmic devices. Based in Washington, US.
Latest FDA clearance: May 2024. Active since 1999.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Optos Plc.
15 devices
Cleared
May 09, 2024
P200TE (A10700)
Ophthalmic
182d
Cleared
Aug 18, 2023
P200TE (A10700)
Ophthalmic
71d
Cleared
Jul 31, 2019
P200TxE
Ophthalmic
132d
Cleared
Feb 28, 2018
P200TE
Ophthalmic
86d
Cleared
Feb 08, 2017
OptosAdvance 4.0 Software
Ophthalmic
201d
Cleared
Jan 16, 2015
P200DTx
Ophthalmic
105d
Cleared
Apr 11, 2014
DAYTONA ICG (P200TICG)
Ophthalmic
101d
Cleared
Feb 22, 2013
OPTOS OCT/SLO MICROPERIMETER
Ophthalmic
323d
Cleared
May 25, 2012
OPTOS ADVANCE
Ophthalmic
161d
Cleared
Aug 19, 2011
P200T
Ophthalmic
70d
Cleared
Sep 30, 2010
P200MAAF
Ophthalmic
30d
Cleared
Jul 15, 2010
OPTOS LIMITED PANORAMIC 200CAF
Ophthalmic
132d