Data / Medical devices / United States / Neuromechanical Innovations, LLC
Neuromechanical Innovations, LLC: FDA-registered device maker in Phoenix, AZ, United States, 2 510(k) clearances
Neuromechanical Innovations, LLC is registered with the FDA (registration 3004620782) in Phoenix, AZ, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 11, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004620782
- Address
- 9831 S 51st St Ste D131, Phoenix, AZ, United States, 85044
- Owner or operator
- NEUROMECHANICAL INNOVATIONS, LLC (9053388)
- Roles
- Manufacturer
- First device listed
- December 10, 2007
- Registered through
- 2026
- Brand names listed
- CBP Adjusting Instrument, Impulse Adjusting Instrument, Impulse iQ Adjusting Instrument, Neuromechanical Adjusting Instrument, ProAdjuster SRT, ProSoft GT, ProSports 360
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Manipulator, Plunger-Like Joint | LXM | U | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| April 11, 2008 | K080261 | IMPULSE IQ ADJUSTING INSTRUMENT | LXM | Substantially Equivalent | Neuromechanical Innovations, LLC | accessdata.fda.gov |
| January 13, 2003 | K023462 | IMPULSE-ADJUSTING INSTRUMENT, CBP ADJUSTING INSTRUMENT, NEUROMECHANICAL ADJUSTING INSTRUMENT, MODELS 2003 | LXM | Substantially Equivalent | Neuromechanical Innovations, LLC | accessdata.fda.gov |
Compare with other makers
Updated April 11, 2008. 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.