Regeneration Technologies, Inc.
FDA 510(k) medical device clearances.
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.