Geistlich-Pharma

FDA Regulatory Profile

Geistlich-Pharma appears in FDA public data with 0 recalls, 16 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 15, 2004.

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K033815BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGENJanuary 15, 2004
K014289ORTHOSS RESORBABLE BONE VOID FILLERMarch 28, 2002
K970569BIO-BLOCKSAugust 14, 2000
K974399BIO-OSS COLLAGENSeptember 16, 1998
K970321BIO-OSS ANORGANIC BOVINE BONESeptember 15, 1998
K972817RESOR-PIN RESORBABLE MEMBRANE PINJuly 24, 1998
K960724BIO-GIDE RESORBABLE BILAYER MEMBRANEJune 11, 1997
K952619BIO-OSS CERAMICAugust 28, 1995
K952618BIO-OSSAugust 28, 1995
K952617BIO-OSSAugust 7, 1995
K920508BIO-OSS BLOCKSNovember 24, 1992
K874943SONAR-AID(R) ULTRASOUND STANDOFF PADJuly 25, 1988
K873763BIO-OSS - CERAMIC PURE NATURAL HYDROXYAPATITEDecember 8, 1987
K871773BIO-OSS PURE NAT HYDROXYAPATITE ENDOSS IMPLANTAugust 24, 1987
K850819GELIPERM ABSORBIND GRANULATED GELMay 7, 1985
K823225GELIPERM GRANULESAugust 12, 1983