# K082218: Max Adjusting Instrument

- Pathway: 510(k) (Traditional)
- Applicant: Manna Omni International, Inc.
- Decided: Aug 13, 2008 after 7 days
- Product code: LXM (Manipulator, Plunger-Like Joint)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K930431 (1994). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080261: Impulse IQ Adjusting Instrument, Neuromechanical Innovations, LLC (2008) Summary page 1.
- K072519: Activator V Spinal Adjusting Instrument, Activator Methods International, Ltd. (2007) Summary page 1.
- K010851: Harrison Hand Held Adjusting Instrument, Harrison Cbp Seminars (2001) Summary page 1.

## Indications for use
MAX is indicated for chiropractic adjustment of the spine and/or extremities. MAX should be used by a licensed health care professional only. Intended for external use only.

Source page: https://510kreport.com/device/K082218
Methodology: https://510kreport.com/methodology