Smith & Nephew Dyonics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 22
What Smith & Nephew Dyonics, Inc. makes
Smith & Nephew Dyonics, Inc. makes arthroscopic surgical blades, fixation screws, and related instrumentation for minimally invasive procedures. Their product line includes disposable arthroscopic blades, cannulated interference screw systems, ligament release systems such as the Ectra II, endoscopic carpal tunnel release systems, posteromedial guides, suction control footswitches with speed control, and arthroscopy inflow and laparoscopy systems.
The devices listed are classified as Class II medical devices and are registered in the FDA 510(k) database. The company is based in the United States.
Catalogue
Search and filter all 22 devicesFrequently asked questions
How many devices does Smith & Nephew Dyonics, Inc. have in the registry?
The registry currently lists 22 devices for Smith & Nephew Dyonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smith & Nephew Dyonics, Inc.'s devices?
Among its 22 most recently registered devices, Smith & Nephew Dyonics, Inc. has devices listed in FDA 510(k) (22 devices).
What risk classes do Smith & Nephew Dyonics, Inc.'s devices fall under?
Among its 22 most recently registered devices, the classes recorded for Smith & Nephew Dyonics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Smith & Nephew Dyonics, Inc. in the registry?
The most recently registered devices listed for Smith & Nephew Dyonics, Inc. include DYONICS FIXATION SCREWS, SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL, ECTRA II LIGAMENT RELEASE SYSTEM and MODIFIED ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM.