Medical Device Manufacturer · SE , Stockholm

Procera Sandvik AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

Total

Cleared

Denied

Procera Sandvik AB has 1 FDA 510(k) cleared medical devices. Based in Stockholm, SE.

Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Dental.

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

Procera Sandvik 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 - Procera Sandvik AB

1 devices

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