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ProAdjuster Kidz

FDA UDI

Class U (US FDA UDI)

by Neuromechanical Innovations, L.L.C.

Identity

Trade Name
ProAdjuster Kidz 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 multiple thrusts over manually selectable force settings. FDA UDI
Model / Reference
ProAdjuster Kidz 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 multiple thrusts over manually selectable force settings. FDA UDI

Identifiers

Primary DI / UDI-DI
00860011416494 FDA UDI
510(k) Number
K023462 FDA UDI
FDA Product Code
LXM FDA UDI
GMDN Term
Joint/spinal manipulator, electronic FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
Not 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

ProAdjuster Kidz by Neuromechanical Innovations, L.L.C. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K023462 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neuromechanical Innovations, L.L.C.

Sources (1)

  • FDA UDI 58edabe5-7f69-4597-a14f-539b98245de4 35 fields · synced May 30, 2026