Axiom Worldwide, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Axiom Worldwide, Inc. makes
Axiom Worldwide, Inc. manufactures spinal decompression devices, including the AXIOM NVP8500, DRX 2000, AXIOM EPS8000, and DRX9000 TRUE SPINAL DECOMPRESSION SYSTEM.
The company's devices are Class II and listed in the FDA 510(k) registry. Axiom Worldwide is based in the US.
Catalogue
Axiom NVP8500 Ref K051135
510(k) 510(k)Drx 2000 Ref K010292
510(k) 510(k)Axiom EPS8000 Ref K050687
510(k) 510(k)DRX9000 True Spinal Decompression System Ref K060735
510(k) 510(k)
Frequently asked questions
How many devices does Axiom Worldwide, Inc. have in the registry?
The registry currently lists 4 devices for Axiom Worldwide, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Axiom Worldwide, Inc.'s devices?
Among its 4 most recently registered devices, Axiom Worldwide, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Axiom Worldwide, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Axiom Worldwide, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Axiom Worldwide, Inc. in the registry?
The most recently registered devices listed for Axiom Worldwide, Inc. include AXIOM NVP8500, DRX 2000, AXIOM EPS8000 and DRX9000 TRUE SPINAL DECOMPRESSION SYSTEM.