Medical Device Manufacturer · NL , Hengelo

Ultrasun International B.V. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
1
Total
1
Cleared
0
Denied

Ultrasun International B.V. has 1 FDA 510(k) cleared medical devices. Based in Hengelo, NL.

Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Ultrasun International B.V. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Bentley Biomedical Consulting, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Ultrasun International B.V.
1 devices
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