Osteogenics Biomedical, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Osteogenics Biomedical, Inc. has 8 FDA 510(k) cleared medical devices. Based in Lubbock, US.
Last cleared in 2021. Active since 1999. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Osteogenics Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Osteogenics Biomedical, Inc.
8 devices
Cleared
Jan 23, 2021
Cytoplast Titanium-Reinforced PTFE Membranes
Dental
267d
Cleared
Oct 19, 2017
RPM Reinforced PTFE Mesh
Dental
127d
Cleared
Mar 01, 2010
PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT#
Dental
89d
Cleared
Oct 31, 2007
CYTOPLAST PTFE SUTURE
General & Plastic Surgery
93d
Cleared
May 16, 2002
IMMIX BONE GRAFT EXTENDER
General & Plastic Surgery
184d
Cleared
Nov 24, 2000
CYTOPLAST SUTURE
General & Plastic Surgery
57d
Cleared
Mar 02, 2000
CYTOPLAST RESORB, MODELS R-250, RP-250, RU-250, RPS-250, RPL-250
Dental
129d
Cleared
Feb 04, 1999
OSTEO-MESH TM-300
Dental
71d