# K152480: Revitive Medic; Revitive MV; Revitive LV

- Pathway: 510(k) (Traditional)
- Applicant: Actegy, Ltd.
- Decided: Mar 31, 2016 after 213 days
- Product code: NGX (Stimulator, Muscle, Powered, For Muscle Conditioning)
- 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
• To temporarily increase local blood circulation in healthy leg muscles • To stimulate healthy muscles in order to improve and facilitate muscle performance. • For temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, upper extremities (arms) and lower extremities (legs) due to strain from exercise or normal household duties.

Source page: https://510kreport.com/device/K152480
Methodology: https://510kreport.com/methodology