# K210174: BEMER Therapy Systems, BEMER Classic Set, BEMER Pro-Set

- Pathway: 510(k) (Traditional)
- Applicant: Bemer Int AG
- Decided: Feb 4, 2021 after 13 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
Longest line of descent: 7 generations back to K940301 (1994). 24 ancestors in all.
5 later devices descend from it; 4 cite it directly.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151834: BEMER Classic Set, BEMER Pro-Set, Bemer Int AG (2017) Summary page 4.

## Most influential descendants
- K250896: Aura Wave (2025), 1 descendant of its own
- K220938: Nova HD+ (2023), 1 descendant of its own
- K262788: Nova HD+ (2026), 0 descendants of its own
- K243165: Limfa Therapy System (Limfa Therapy) (2025), 0 descendants of its own
- K231368: Bemer Therapy System Evo (2023), 0 descendants of its own

## 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

Source page: https://510kreport.com/device/K210174
Methodology: https://510kreport.com/methodology