Data / Medical devices / United States / Artheon Orthopedic Devices
Artheon Orthopedic Devices: FDA-registered device maker in La Verne, CA, United States, 1 510(k) clearance
Artheon Orthopedic Devices is registered with the FDA (registration 3027383626) in La Verne, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 10, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3027383626
- Address
- 1888 arrow highway, La Verne, CA, United States, 91750
- Owner or operator
- Artheon Orthopedic Devices (10089360)
- Roles
- Specification developer
- First device listed
- February 6, 2024
- Registered through
- 2026
- Brand names listed
- X Force Stimulator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Electrical, Transcutaneous, For Arthritis | NYN | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 10, 2011 | K111557 | X-FORCE | NYN | Substantially Equivalent | Seven Seas Distribtion and Manufacturing, LLC | accessdata.fda.gov |
Compare with other makers
Updated November 10, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.