Talia Technology , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Talia Technology , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Talia Technology , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 6 cleared submissions from 1994 to 2006. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Talia Technology , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Talia Technology , Ltd.
6 devices
Cleared
Aug 23, 2006
RTA 5 & RTA MODEL E RETINAL THICKNESS ANALYZER
Ophthalmic
70d
Cleared
May 24, 2004
RTA MODEL D RETINAL THICKNESS ANALYZER
Ophthalmic
11d
Cleared
May 06, 2003
RTA MODEL D RETINAL THICKNESS ANALYZER
Ophthalmic
12d
Cleared
Mar 31, 2000
MODIFICATION TO RTA RETINAL THICKNESS ANALYZER
Ophthalmic
25d
Cleared
Feb 03, 1997
RTA RETINAL THICKNESS ANALYZER
Ophthalmic
111d
Cleared
Jan 25, 1994
TALIA LASER SLIT
Ophthalmic
358d