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The Straumann Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K041070STRAUMANN TEMPORARY COPINGJuly 23, 2004
K040646STRAUMANN GRANULESMay 3, 2004
K040469THE STRAUMANN ORTHO IMPLANT SYSTEMApril 30, 2004
K993862MODUS SAGITTAL SPLIT PLATEDecember 29, 1999
K962023PLASTIC PROTECTION HEALING CAPSAugust 15, 1996
K960634TITANIUM HEALING CAPSJune 18, 1996
K955281ENDOSSEOUS DENTAL IMPLANT & ACCESSORIESMarch 15, 1996
K955369MEMFIXJanuary 23, 1996
K941393ITI ANGLED ABUTMENTJune 14, 1995
K943720ITI TRANSVERSAL SCREWING SYSTEMMarch 24, 1995
K931993ITI DISTANCE SYSTEMApril 26, 1994
K923872BONE MARROW BIOPSY SYSTEMDecember 15, 1992
K920928PRE-STERILIZED ITI DENTAL IMPLANTSJuly 15, 1992
K920768HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MMApril 21, 1992