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OSTEOGENICS BIOMEDICAL, INC.

Last updated September 17, 2026

Information

Country: US
Address: 4620 71st St Bldg 78-79, LUBBOCK, TX, 79424
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3002253367
DUNS Number: —

Catalogue (326)

Page 3 of 7

Device	Model / Reference	Registries	Class	Status
Cytoplast™ PTFE Suture	CS052819BKSS	FDA UDI	Class II	Active
Osteo-Mesh Tm-300	TM4545	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0418	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200PDMR	FDA UDI	Class II	Active
Cytoplast Rtm Collagen	RTM3040-1	FDA UDI	Class II	Unknown
Pro-fix™ Precision Fixation System	PFT5-5	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250AS-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250K2	FDA UDI	Class II	Unknown
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PS-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250XLK-N-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PTC-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0618PREMSS	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFMK20	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250XL-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200ATCM	FDA UDI	Class II	Active
Zcore	ZY100	FDA UDI	Class II	Unknown
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150ATC-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0518BK	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150ANL-N-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250XL-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PTC-N-2	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200BLL	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PTC-N-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150K2-N-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250ATC	FDA UDI	Class II	Unknown
Pro-fix™ Precision Fixation System	PFBK12	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PS-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PL	FDA UDI	Class II	Unknown
Pro-fix™ Precision Fixation System	PFB8-5	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFT3	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250ATCM	FDA UDI	Class II	Unknown
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250AP-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFT10	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200K2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PP-2	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PTCM	FDA UDI	Class II	Unknown
Cytoplast™ PTFE Suture	CS0518BKSS	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS072813	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS071813SS	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0523SS	FDA UDI	Class II	Active
X-Gut™ Chromic Gut Suture	GC401975	FDA UDI	Class II	Active
Cytoplast Rtm Collagen	RTM1520-1	FDA UDI	Class II	Unknown
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250ANL30-N-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PLT-N-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFMF-5	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150BL-N-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PST-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150K2-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250XLK-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200XLK	FDA UDI	Class II	Active

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Sep 7, 2016	Z-0113-2017	—	terminated	The device has the potential to be packaged in the wrong product box.