Regeneration Technologies, Inc.
Regeneration Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2008.
Top product codes for Regeneration Technologies, Inc.
Recent clearances by Regeneration Technologies, Inc.
- K080418 — REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST
- K072238 — BIOSET XCH
- K072327 — CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON
- K063584 — STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937
- K060180 — BIOSET XC
- K060253 — STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST.
- K052405 — STERLING INTERFERENC SCREW HT
- K051615 — STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES
- K050767 — STERLING INTERFERENCE SCREW ST
- K043421 — OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP IC
- K043420 — OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTE
Data sourced from openFDA. This site is unofficial and independent of the FDA.