# Medisiss

- Location (FDA's records): Redmond, OR
- FDA decisions: 6 (2003–2011): 6 510(k) clearances
- Product codes: GEI (2), NLQ (1), HRX (1), NLR (1), NON (1)
- Predicates its devices cite: 23 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrocare Corp.: 4 (https://510kreport.com/company/arthrocare)
- Ethicon Endo-Surgery, Inc.: 3 (https://510kreport.com/company/ethicon-endo-surgery)
- Surgical Instruments Service and Savings, Inc.: 2 (https://510kreport.com/company/surgical-instruments-service-and-savings)
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Olympus Optical Co., Ltd.: 1 (https://510kreport.com/company/olympus-optical)
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)
- Conmedcorp: 1 (https://510kreport.com/company/conmedcorp)
- Megadyne Medical Products, Inc.: 1 (https://510kreport.com/company/megadyne-medical-products)

## Recent decisions
- K113028: Medisiss Reprocessed Arthroscopic Shavers and Burs (Dec 20, 2011)
- K100543: Medississ Reprocessedent Ablation Wands (Coblators), Model#EIC8872-01 (Jul 23, 2010)
- K081559: Genesis (Aug 28, 2008)
- K042659: Medisiss Reprocessed Non-Electric GI Biopsy Forceps (Feb 14, 2005)
- K030598: Medisiss Reprocessed Ultrasonic Surgical Instruments (Jan 23, 2004)
- K030919: Siss, Inc. (D.B.a.Medisiss) Reprocessd Electrosurgical Instruments and Accessories (Jul 3, 2003)

Source page: https://510kreport.com/company/medisiss