Medisiss
Country not established
- Devices
- 6
What Medisiss makes
Medisiss reprocesses single-use electrosurgical instruments and accessories, including arthroscopic shavers and burs, ultrasonic surgical tools, GI biopsy forceps, and coblation ablation wands. Their portfolio also covers reprocessed reusable devices like electrosurgical instruments and arthroscopic equipment, ensuring they meet surgical and procedural needs across multiple specialties.
The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with regulatory submissions recorded in the FDA’s 510(k) database. Their products are listed in the United States, where Medisiss is based.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Genesis Ref K081559
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medisiss have in the registry?
The registry currently lists 6 devices for Medisiss. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medisiss's devices?
Among its 6 most recently registered devices, Medisiss has devices listed in FDA 510(k) (6 devices).
What risk classes do Medisiss's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Medisiss's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medisiss in the registry?
The most recently registered devices listed for Medisiss include SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURS, MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS and GENESIS.