NEUROMECHANICAL INNOVATIONS, LLC

FDA Device Registration & Listing · Phoenix, AZ, US · Registration 3004620782

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004620782
FEI Number
3004620782
Entity Name
NEUROMECHANICAL INNOVATIONS, LLC
City/State/Country
Phoenix, AZ, US
Establishment Address
9831 S 51st St Ste D131, Phoenix, AZ 85044, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NEUROMECHANICAL INNOVATIONS, LLC (Owner Number: 9053388)
Owner / Operator Contact Address
9831 S 51st St, Suite D131, --, Phoenix, AZ 85044, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K023462
PMA Number
N/A

All Registered Proprietary Names

Impulse iQ Adjusting Instrument Impulse Adjusting Instrument CBP Adjusting Instrument Neuromechanical Adjusting Instrument ProAdjuster SRT ProSoft GT ProSports 360

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXM Manipulator, Plunger-Like Joint Unknown Class U N/A 2008-11-03
LXM Manipulator, Plunger-Like Joint Unknown Class U N/A 2007-12-10

Official Correspondent

CHRISTOPHER COLLOCA, DC, PhD

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NEUROMECHANICAL INNOVATIONS, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004620782. Last updated year: 2026. Please use registration number 3004620782 when referencing this establishment in official correspondence.
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