Identity
- Trade Name
- Impulse iQ Adjusting Instrument FDA UDI
- Generic Name
- Joint/spinal manipulator, electronic FDA UDI
- Device Name
- Chiropractic adjusting instrument; Hand-held medical manipulation/mobilization device for the intended use of manipulation/mobilization of musculoskeletal joints that provides impulsive single and variable frequency multiple thrusts over three selectable force settings. FDA UDI
- Model / Reference
- iQ FDA UDI
- Description
- Chiropractic adjusting instrument; Hand-held medical manipulation/mobilization device for the intended use of manipulation/mobilization of musculoskeletal joints that provides impulsive single and variable frequency multiple thrusts over three selectable force settings. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860011416418 FDA UDI
- 510(k) Number
- K080261 FDA UDI
- FDA Product Code
- LXM FDA UDI
- GMDN Term
- Joint/spinal manipulator, electronic FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Joint/spinal manipulator, electronic
Impulse iQ Adjusting Instrument by Neuromechanical Innovations, L.L.C. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
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Manufacturer
- Manufacturer
- Neuromechanical Innovations, L.L.C.
Sources (1)
- FDA UDI 452603d3-7b58-49f2-8c58-42721aed9b56 35 fields · synced May 30, 2026