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Lifecore Biomedical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
34
Inspections
8
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K073032PRIMACONNEX SD ESTHETIC CONTOUR ZI ABUTMENTSNovember 16, 2007
K072241PRIMACONNEX CAD/CAM ABUTMENT SYSTEMNovember 9, 2007
K072768RESTORE, STAGE-1, RENOVA PRIMASOLO AND PRIMACONNEX DENTAL IMPLANTSOctober 23, 2007
K072572PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTSOctober 5, 2007
K062876PRIMACONNEX CERAMIC ABUTMENTSNovember 1, 2006
K060530SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LMay 22, 2006
K053643STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026January 23, 2006
K051614PRIMACONNEX INTERNAL CONNECTION IMPLANT SYSTEM, PRIMACONNEX INTERNAL CONNECTION PROSTHETICSSeptember 9, 2005
K050506PRIMASOLO ONE-PIECE IMPLANTS & HEALING CAPSApril 15, 2005
K041324CALMATRIX CALCIUM SULFATE BONE GRAFT BINDERJuly 19, 2004
K032774RENOVA INTERNAL HEX IMPLANT SYSTEMNovember 26, 2003
K032495THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEMSeptember 17, 2003
K002037LIFECORE BIOMEDICAL DENTAL IMPLANT SYSTEMSMay 16, 2001
K003226THE LIFECORE STAGE-1 SINGLE STAGE RBM DENTAL IMPLANT SYSTEMJanuary 12, 2001
K993894LIFECORE SINGLE TOOTH ABUTMENT SYSTEMMarch 8, 2000
K994205MODIFICATION OF REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEMFebruary 29, 2000
K991114REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEMJuly 14, 1999
K970776LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENTMay 27, 1997
K965135LIFECORE CONICAL ABUTMENTFebruary 25, 1997
K961511HAPSET HYDROXYLAPATITE BONE GRAFT PLASTERJune 28, 1996