Medical Device Manufacturer · SE , Sweden

Ultra Tan Intl. AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

Ultra Tan Intl. AB has 2 FDA 510(k) cleared medical devices. Based in Sweden, SE.

Historical record: 2 cleared submissions from 1988 to 1988. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Ultra Tan Intl. AB Filter by specialty or product code using the sidebar.

Ultra Tan Intl. AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ultra Tan Intl. AB

2 devices

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