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Regeneration Technologies, Inc.

11 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST (K080418)Regeneration Technologies, Inc.2008-04-30
BIOSET XCH (K072238)Regeneration Technologies, Inc.2008-01-25
CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON (K072327)Regeneration Technologies, Inc.2007-10-24
STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937 (K063584)Regeneration Technologies, Inc.2007-05-09
BIOSET XC (K060180)Regeneration Technologies, Inc.2006-09-06
STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST. (K060253)Regeneration Technologies, Inc.2006-02-23
STERLING INTERFERENC SCREW HT (K052405)Regeneration Technologies, Inc.2005-11-16
STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES (K051615)Regeneration Technologies, Inc.2005-08-15
STERLING INTERFERENCE SCREW ST (K050767)Regeneration Technologies, Inc.2005-06-09
OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP IC (K043421)Regeneration Technologies, Inc.2005-02-16
OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTE (K043420)Regeneration Technologies, Inc.2005-02-10

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Every clearance here is in the API, with alerts when new ones post.