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Activator Methods

FDA UDI

Class U (US FDA UDI)

by Activator Methods International Ltd.

Identity

Trade Name
Activator Methods FDA UDI
Generic Name
Joint/spinal manipulator, mechanical FDA UDI
Device Name
Chiropractic Adjusting Instrument FDA UDI
Model / Reference
EZIV FDA UDI
Description
Chiropractic Adjusting Instrument FDA UDI

Identifiers

Primary DI / UDI-DI
00850021303051 FDA UDI
510(k) Number
K003185 FDA UDI
FDA Product Code
LXM FDA UDI
GMDN Term
Joint/spinal manipulator, mechanical 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Joint/spinal manipulator, mechanical

Activator Methods by Activator Methods International Ltd. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Joint/spinal manipulator, mechanical.

Cleared under the same submission

K003185 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Activator Methods International Ltd.

Sources (1)

  • FDA UDI e670b7f2-f6e4-4e8e-a75e-53e6d5f6f575 34 fields · synced May 30, 2026