Medical Device Manufacturer · US , Alachua , FL

Regeneration Technologies, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2005

Total

Cleared

Denied

Regeneration Technologies, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Alachua, US.

Historical record: 11 cleared submissions from 2005 to 2008.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Regeneration Technologies, Inc.

11 devices

1-11 of 11

Cleared Apr 30, 2008

REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS...

CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON

K072327 · MQV

Orthopedic · 65d

Cleared May 09, 2007

STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL...

STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST.

K060253 · HWC

Orthopedic · 22d

Cleared Nov 16, 2005

STERLING INTERFERENC SCREW HT

K052405 · HWC

Orthopedic · 76d

Cleared Aug 15, 2005

STERLING CANCELLOUS CHIPS

K051615 · MQV

Orthopedic · 59d

Cleared Jun 09, 2005

STERLING INTERFERENCE SCREW ST

K050767 · HWC

Orthopedic · 76d

Cleared Feb 16, 2005

OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP IC

K043421 · MQV

Orthopedic · 65d

Cleared Feb 10, 2005

OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTE

K043420 · MQV

Orthopedic · 59d

Regeneration Technologies, Inc. - FDA 510(k) Cleared Devices

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