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.

Ivoclar North America, Inc.

FDA 510(k) & PMA Approved Devices — 131 products

Total Devices131
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K012174 ERIS LAYERING MATERIALSEIH2001-08-27 View
510(k) K011491 HELIOSEAL CLEAR CHROMAEBC2001-08-16 View
510(k) K011492 IN TEN-SEBF2001-07-05 View
510(k) K011490 MODIFICATION TO EXCITEKLE2001-06-27 View
510(k) K011022 BIOUNIVERSAL PDFEJT2001-05-02 View
510(k) K011023 D.SIGN 96EJT2001-05-02 View
510(k) K010381 D.SIGN 30EJH2001-03-06 View
510(k) K010250 TETRIC CERAM HBEBF2001-02-28 View
510(k) K003293 EXCITE DSCKLE2001-02-06 View
510(k) K003407 SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER)EMA2001-01-26 View
510(k) K003635 DW 276 #3EJT2000-12-22 View
510(k) K003634 DW 272 #1EJT2000-12-21 View
510(k) K003633 DW 277 #4EJT2000-12-20 View
510(k) K003632 DW 273 #1EJS2000-12-20 View
510(k) K003377 FERMIT N PLUSEBG2000-12-04 View
510(k) K003374 FERMIT PLUSEBG2000-12-04 View
510(k) K003373 PROCAD ADD-ONEIH2000-11-28 View
510(k) K002872 R&D PROJECT DW271#11AEJT2000-11-02 View
510(k) K001469 R&D PROJECT DW269#25EJS2000-07-05 View
510(k) K993783 TETRIC FLOWEBF1999-12-13 View
↑