Medical Device Manufacturer · SE , 931 27 Skellettea

Dentronic AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999

Total

Cleared

Denied

Dentronic AB has 1 FDA 510(k) cleared medical devices. Based in 931 27 Skellettea, SE.

Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Dental.

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

Dentronic 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 - Dentronic AB

1 devices

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