Medical Device Manufacturer · US , Sisters , OR

Medisiss - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2003

Recent clearances: MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURS, MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01, GENESIS

6

Total

6

Cleared

0

Denied

Medisiss has 6 FDA 510(k) cleared medical devices. Based in Sisters, US.

Historical record: 6 cleared submissions from 2003 to 2011. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Medisiss Filter by specialty or product code using the sidebar.

Medisiss is one of 15145 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medisiss

6 devices

1-6 of 6

Cleared Dec 20, 2011

MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURS

Orthopedic · 70d

Cleared Jul 23, 2010

MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01

General & Plastic Surgery · 148d

Cleared Aug 28, 2008

General & Plastic Surgery · 86d

Cleared Feb 14, 2005

MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS

Gastroenterology & Urology · 139d

Cleared Jan 23, 2004

MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS

General & Plastic Surgery · 332d

Cleared Jul 03, 2003

SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND...

Gastroenterology & Urology · 101d