# K123354: Revitive IX

- Pathway: 510(k) (Traditional)
- Applicant: Actegy, Ltd.
- Decided: Jun 28, 2013 after 240 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K932299 (1994). 11 ancestors in all.
19 later devices descend from it; 2 cite it directly.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050046: Rehabilicare IF 3 Wave Interferential Stimulator System, Model 7110S, Compex Technologies, Inc. (2005) Summary page 1.
- K103719: Lifecare Conductive Garments, Everyway Medical Instruments Co.,Ltd (2011) Summary page 1.

## Most influential descendants
- K143207: Revitive IX (OTC) (2015), 17 descendants of its own
- K151834: BEMER Classic Set, BEMER Pro-Set (2017), 11 descendants of its own
- K210174: BEMER Therapy Systems, BEMER Classic Set, BEMER Pro-Set (2021), 5 descendants of its own
- K203710: Storz Medical MAGNETOLITH Muscle Stimulator (2021), 4 descendants of its own
- K240234: BTL-899MS (2024), 2 descendants of its own

## Indications for use
The Revitive IX device is indicated for: Relaxation of muscle spasms Prevention or retardation of disuse atrophy Increasing local blood circulation Muscle re-education Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis Maintaining or increasing range of motion

Source page: https://510kreport.com/device/K123354
Methodology: https://510kreport.com/methodology