# K072252: Veinoplus Neuromuscular Stimulator

- Pathway: 510(k) (Traditional)
- Applicant: Ad Rem Technology Sarl
- Decided: Jan 30, 2008 after 170 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: 1 generation back to K022175 (2002). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022175: P4 Physio, Valmed Corp. (2002) Summary page 2.

## Cited in the summary but kept off the family tree
- K040253: Easy Med TN-28 C, Easy Med Instrument Co., Ltd. (2004). Our reading of the summary gave K040253, FDA’s number for Easy Med TN-28 C (Easy Med Instrument Co., Ltd.). Its FDA name has none of the distinctive words the summary uses for the device it names, “EASYMED TN-28C T.E.N.S. Unit”. Kept off the family tree. Summary page 3.

## Most influential descendants
- K141919: Veinoplus Sport Neuromuscular Stimulator (2015), 0 descendants of its own

## Indications for use
The VEINOPLUS Neuromuscular Stimulator is indicated for the following: In the Primary Mode of Action (PMOA) when the Operating Mode number 1 for muscle stimulation is activated, the Indications for Use are: * Relaxation of muscle spasms. * Prevention or retardation of muscle 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. In the other Mode of Action (MOA), when the Operating Mode number 2 for Transcutaneous Electrical Nerve Stimulation (TENS) stimulation is activated, the Indication for Use is: Providing symptomatic pain relief for chronic, acute or post operative pain.

Source page: https://510kreport.com/device/K072252
Methodology: https://510kreport.com/methodology