Medyssey USA, Inc.
United StatesFDA applicant, unverified
- Devices
- 19
What Medyssey USA, Inc. makes
Medyssey USA, Inc. manufactures spinal fixation systems, including cervical and lumbar cages, pedicle screw systems, and anterior cervical fusion cages. Their product line covers interbody fusion devices like the Triton Cage, Medussa-PL Cage, and BN Lumbar Cage System, as well as cervical plating systems such as the Athena III, Athena II, and Athena Cervical Plate Systems. Additional offerings include modular spinal fixation systems like the Zenius, Iliad, and Kora systems, designed for surgical stabilization of the spine.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database, reflecting compliance with U.S. medical device authorization requirements. Medyssey USA, Inc. is based in the United States.
Catalogue
Search and filter all 19 devicesFrequently asked questions
How many devices does Medyssey USA, Inc. have in the registry?
The registry currently lists 19 devices for Medyssey USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medyssey USA, Inc.'s devices?
Among its 19 most recently registered devices, Medyssey USA, Inc. has devices listed in FDA 510(k) (19 devices).
What risk classes do Medyssey USA, Inc.'s devices fall under?
Among its 19 most recently registered devices, the classes recorded for Medyssey USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medyssey USA, Inc. in the registry?
The most recently registered devices listed for Medyssey USA, Inc. include Zenius™ Spinal System, Triton Cage, Medussa-PL Cage and BN LUMBAR CAGE SYSTEM.