Dyonics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 19
What Dyonics, Inc. makes
Dyonics, Inc. manufactures arthroscopic surgical instruments and accessories, including cannulas, trocars, saw blades, shavers, and disposable blades for joint procedures. Their portfolio covers shoulder and knee surgical systems, such as the PS3500 and Pacesetter 3500 arthroscopic systems, as well as specialized tools like ligament repair kits and drill guides for intra-articular procedures.
The company’s devices are regulated under FDA 510(k) clearance, spanning Class I and Class II classifications. Products are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Search and filter all 19 devicesFrequently asked questions
How many devices does Dyonics, Inc. have in the registry?
The registry currently lists 19 devices for Dyonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dyonics, Inc.'s devices?
Among its 19 most recently registered devices, Dyonics, Inc. has devices listed in FDA 510(k) (19 devices).
What risk classes do Dyonics, Inc.'s devices fall under?
Among its 19 most recently registered devices, the classes recorded for Dyonics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dyonics, Inc. in the registry?
The most recently registered devices listed for Dyonics, Inc. include MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES, PS3500 ARTHROSCOPIC SURGICAL SYSTEM, MODIFIED SAW BLADES TO THE SAGITAL SAW and MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM.