ClearanceBrief
Company ยท US

Medisiss

FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2011. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEIElectrosurgical, Cutting & Coagulation & Accessories2
HRXArthroscope1
NLQSingle-Use Reprocessed Ultrasonic Surgical Instruments1
NLRUnit, Electrosurgical, Endoscopic (With Or Without Accessories), Reprocessed1
NONForceps, Biopsy, Non-Electric, Reprocessed1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 20, 2011K113028MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURS
Medisiss
HRX
Jul 23, 2010K100543MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01
Medisiss
GEI
Aug 28, 2008K081559GENESIS
Medisiss
GEI
Feb 14, 2005K042659MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS
Medisiss
NON
Jan 23, 2004K030598MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS
Medisiss
NLQ
Jul 3, 2003K030919SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES
Medisiss
NLR

Latest recalls

DateFirm and productCodeLinked 510(k)
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