Medisiss

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K113028MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURSDecember 20, 2011
K100543MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01July 23, 2010
K081559GENESISAugust 28, 2008
K042659MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPSFebruary 14, 2005
K030598MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTSJanuary 23, 2004
K030919SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIESJuly 3, 2003