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Regeneration Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K080418REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET ICApril 30, 2008
K072238BIOSET XCHJanuary 25, 2008
K072327CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTONOctober 24, 2007
K063584STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937May 9, 2007
K060180BIOSET XCSeptember 6, 2006
K060253STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST.February 23, 2006
K052405STERLING INTERFERENC SCREW HTNovember 16, 2005
K051615STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBESAugust 15, 2005
K050767STERLING INTERFERENCE SCREW STJune 9, 2005
K043421OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP ICFebruary 16, 2005
K043420OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTEFebruary 10, 2005