Katalyst Surgical, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Katalyst Surgical, LLC has 7 FDA 510(k) cleared medical devices. Based in Washington, US.
Last cleared in 2022. Active since 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Katalyst Surgical, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Katalyst Surgical, LLC
7 devices
Cleared
Oct 07, 2022
Kogent Disposable Copper Forceps, Kogent Disposable Irrigating Copper...
General & Plastic Surgery
326d
Cleared
Jun 19, 2020
Kogent Torus Ultrasonic Aspirator
General & Plastic Surgery
240d
Cleared
Jun 15, 2017
Katalyst Cyclophotocoagulation Probe
Ophthalmic
175d
Cleared
Apr 09, 2015
KOGENT SPETZLER LIGHTED SUCTION TUBES
General & Plastic Surgery
281d
Cleared
Sep 15, 2014
KATALYST REVOLVER LASER PROBES, KATALYST REVOLVER ILLUMINATED LASER PROBES,...
Ophthalmic
215d
Cleared
Dec 21, 2012
KOGENT BIPOLAR FORCEPS
General & Plastic Surgery
73d
Cleared
Sep 17, 2012
KATALYST LASER PROBES, KATALYST ILLUMINATED LASER PROBES
Ophthalmic
151d