ClearanceBrief
Company ยท US

Keeler Limited

FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2015. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HKYTonometer, Manual4
HJOBiomicroscope, Slit-Lamp, Ac-Powered3
HKICamera, Ophthalmic, Ac-Powered1
HRNUnit, Cryophthalmic, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 31, 2015K152644KEELER DISPOSABLE TONOMATE, KEELER DISPOSABLE TONOMATE, BOX OF 100
Keeler Limited, GB
HKY
Sep 10, 2015K151394Keeler Slit Lamp
Keeler Limited, GB
HJO
Sep 17, 2014K142179D-KAT Z-YPE
Keeler, Ltd.
HKY
Jul 11, 2014K140451KEELER SLIT LAMP H-SERIES DIGITAL (HALOGEN BULB OPTION), KEELER SLIT LAMP H-SERIES DIGITAL (LED OPTION)
Keeler Limited
HJO
Jun 17, 2014K140450KEELER KAPTURE SOFTWARE
Keeler Limited
HKI
Feb 21, 2014K133234T-TYPE D-KAT, R-TYPE D-KAT
Keeler Limited
HKY
Dec 23, 2013K131787CRYOMATIC MKII CONSOLE, CRYOMATIC MKII PROBES, DISPOSABLE CRYO PROBES
Keeler, Ltd.
HRN
Jun 27, 2013K131589KEELER SLIT LAMP H-SERIES
Keeler, Ltd., GB
HJO
Jan 19, 2010K093445KEELER APPLANATION TONOMETER; T-TYPE KAT, K-TYPE KAT, (KAT)
Keeler, Ltd.
HKY

Latest recalls

DateFirm and productCodeLinked 510(k)
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