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Khan Kinetic Treatment Device (KKT-M2)

FDA UDI

Class U (US FDA UDI)

by Optima Health Solutions International, Inc.

Identity

Trade Name
Khan Kinetic Treatment Device (KKT-M2) FDA UDI
Generic Name
Physical therapy ultrasound system FDA UDI
Device Name
The KKT-M2 device is to be used in the aid of management of chronic pain due to non-congenital defects. The device can be used as part of a series of steps in the total care of the patient. The procedure involves the use of diagnostic imaging that qualifies the misalignment between vertebrae. The treatment is then administered using the KKT-M2 device to deliver precise impulses at a required vector configuration. FDA UDI
Model / Reference
KKT-M2 FDA UDI
Description
The KKT-M2 device is to be used in the aid of management of chronic pain due to non-congenital defects. The device can be used as part of a series of steps in the total care of the patient. The procedure involves the use of diagnostic imaging that qualifies the misalignment between vertebrae. The treatment is then administered using the KKT-M2 device to deliver precise impulses at a required vector configuration. FDA UDI

Identifiers

Catalog Number
M2 FDA UDI
Primary DI / UDI-DI
B854M20 FDA UDI
510(k) Number
K130666 FDA UDI
FDA Product Code
LXM FDA UDI
GMDN Term
Physical therapy ultrasound system 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Physical therapy ultrasound system

Khan Kinetic Treatment Device (KKT-M2) by Optima Health Solutions International, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy ultrasound system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd4dbbfa-4ad2-4e55-9f22-0e35c6846e4c 36 fields · synced May 30, 2026