Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Procera Sandvik, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K010630 Y-TZP POWDER AND PROCERA ALLZIRKONEIH2001-04-17 View
510(k) K001418 ALUMINUM OXIDE POWDER, SUMICORUNDUM AAO4SEIH2000-07-05 View
↑