This page includes the latest FDA filings for Regeneration Technologies Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
REGENERATION TECHNOLOGIES, INC. | REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST | 2008-04-30 |
REGENERATION TECHNOLOGIES, INC. | BIOSET XCH | 2008-01-25 |
REGENERATION TECHNOLOGIES, INC. | CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON | 2007-10-24 |
REGENERATION TECHNOLOGIES, INC. | STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937 | 2007-05-09 |
REGENERATION TECHNOLOGIES, INC. | BIOSET XC | 2006-09-06 |
REGENERATION TECHNOLOGIES, INC. | STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST. | 2006-02-23 |
REGENERATION TECHNOLOGIES, INC. | STERLING INTERFERENC SCREW HT | 2005-11-16 |
REGENERATION TECHNOLOGIES, INC. | STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES | 2005-08-15 |
REGENERATION TECHNOLOGIES, INC. | STERLING INTERFERENCE SCREW ST | 2005-06-09 |
REGENERATION TECHNOLOGIES, INC. | OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP IC | 2005-02-16 |
REGENERATION TECHNOLOGIES, INC. | OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTE | 2005-02-10 |