Endius, Inc.
United StatesFDA applicant, unverified
- Devices
- 33
What Endius, Inc. makes
Endius, Inc. manufactures spinal fixation and endoscopic access devices, including polyaxial and posterior cervical/thoracic fixation systems, spinal endoscopes, and suction/irrigation instruments. Their portfolio also includes modifications to existing systems like the Atavi and endoscopic spinal access platforms, as well as bipolar sheaths for surgical procedures.
The company’s devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. Their products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Search and filter all 33 devicesFrequently asked questions
How many devices does Endius, Inc. have in the registry?
The registry currently lists 33 devices for Endius, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endius, Inc.'s devices?
Among its 33 most recently registered devices, Endius, Inc. has devices listed in FDA 510(k) (33 devices).
What risk classes do Endius, Inc.'s devices fall under?
Among its 33 most recently registered devices, the classes recorded for Endius, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endius, Inc. in the registry?
The most recently registered devices listed for Endius, Inc. include ENDIUS FLEXTIP BLADE, ENDIUS MINIT POSTERIOR CERVICAL AND UPPER THORACIC FIXATION SYSTEM, ENDIUS SPINAL FIXATION SYSTEM and ENDIUS TITLE 2 POLYAXIAL SPINAL SYSTEM.