Medical Device Manufacturer · US , Sisters , OR

Medisiss - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2003

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.

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