Keos
United Statesfrom the FDA registration address FDA FEI 3013921069
- Devices
- 443
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Keos makes
KEOS makes a range of medical devices, including polymeric spinal interbody fusion cages, reusable instrument trays, spinal implant trials, and various reusable orthopaedic tools such as bone curettes, chisels, levers, and files. Examples of their devices include the Lumbar IBFD and Keos Lumbar Instrument.
The company's portfolio is regulated under Class I and Class II devices and is listed in the FDA UDI registry. KEOS is based in the US.
Catalogue
Search and filter all 443 devicesShowing 1-50 of 443
Company details
- FDA FEI number
- 3013921069
- DUNS number
- 080551837
- Address
- 5625 Strand Blvd Ste 505, Naples, FL, 34110
Frequently asked questions
How many devices does KEOS have in the registry?
The registry currently lists 443 devices for KEOS. Devices recorded under merged duplicate company entries are counted once.
Which registries list KEOS's devices?
Among its 50 most recently registered devices, KEOS has devices listed in FDA GUDID (50 devices).
What risk classes do KEOS's devices fall under?
Among its 50 most recently registered devices, the classes recorded for KEOS's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from KEOS in the registry?
The most recently registered devices listed for KEOS include Lumbar IBFD 28L x 10W x 8H Curved, HA, Keos Lumbar Instrument Rotating Distractor, QC, 6mm, Keos Lumbar Instrument and Lumbar IBFD 28L x 10W x 8H Straight, HA.