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FDA 510(k)

VEINOPLUS Back

K-Number: K251958 · 2025-12-23

ApplicantDynapulse Medical
Decision Date2025-12-23
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VEINOPLUS Back is a medical device manufactured by Dynapulse Medical. It received FDA 510(k) clearance on 2025-12-23 under approval number K251958. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEINOPLUS Back?

VEINOPLUS Back is a medical device that received FDA 510(k) clearance on 2025-12-23. It is manufactured by Dynapulse Medical. The 510(k) number is K251958.

When was VEINOPLUS Back approved by the FDA?

VEINOPLUS Back received FDA 510(k) clearance on 2025-12-23, under approval number K251958.

What company makes VEINOPLUS Back?

VEINOPLUS Back is manufactured by Dynapulse Medical.

What is the FDA product code for VEINOPLUS Back?

The FDA product code for VEINOPLUS Back is NUH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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