# K251958: VEINOPLUS Back

- Pathway: 510(k) (Traditional)
- Applicant: Dynapulse Medical
- Decided: Dec 23, 2025 after 181 days
- Product code: NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K130802 (2013). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130802: Otc Electrical Stimulator (MT9001), Otc Tens Device (LT3060), Shenzhen Dongdixin Technology Co., Ltd. (2013) Summary page 5.

## Indications for use
The Veinoplus® Back is to be used for temporary relief of pain associated with sore and aching muscles in the back (shoulder, middle of the back, or lumbar area), due to strain from exercise or normal household and work activities.

Source page: https://510kreport.com/device/K251958
Methodology: https://510kreport.com/methodology