Keeler Limited is one of 12989 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Keeler Limited - FDA 510(k) Cleared Devices
Recent clearances: KEELER DISPOSABLE TONOMATE, KEELER DISPOSABLE TONOMATE, BOX OF 100, Keeler Slit Lamp, KEELER SLIT LAMP H-SERIES DIGITAL (HALOGEN BULB OPTION), KEELER SLIT LAMP H-SERIES DIGITAL (LED OPTION)
5
Total
5
Cleared
0
Denied
Keeler Limited has 5 FDA 510(k) cleared medical devices. Based in Broomall, US.
Historical record: 5 cleared submissions from 2014 to 2015. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Keeler Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Keeler Instruments, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Keeler Limited
5 devices
Cleared
Dec 31, 2015
KEELER DISPOSABLE TONOMATE, KEELER DISPOSABLE TONOMATE, BOX OF 100
Ophthalmic
106d
Cleared
Sep 10, 2015
Keeler Slit Lamp
Ophthalmic
107d
Cleared
Jul 11, 2014
KEELER SLIT LAMP H-SERIES DIGITAL (HALOGEN BULB OPTION), KEELER SLIT LAMP...
Ophthalmic
137d
Cleared
Jun 17, 2014
KEELER KAPTURE SOFTWARE
Ophthalmic
113d
Cleared
Feb 21, 2014
T-TYPE D-KAT, R-TYPE D-KAT
Ophthalmic
123d