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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 2 of 7

Device	Model / Reference	Registries	Class	Status
Cytoplast™ PTFE Suture	CS051819BKSS	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PL-N-2	FDA UDI	Class II	Active
X-Gut™ Plain Gut Suture	GP301975	FDA UDI	Class II	Active
X-Gut™ Plain Gut Suture	GP401945	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFTK12	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150K2-2	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0628RCSS	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PLT-N-2	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PLT	FDA UDI	Class II	Unknown
RPM™ Reinforced PTFE Mesh	RPM250XLKM	FDA UDI	Class II	Unknown
Zcore	ZS400	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PD-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200PLT	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PS-N-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS071816SS	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150XLK-N-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200PL	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PLT-2	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PST	FDA UDI	Class II	Unknown
X-Gut™ Chromic Gut Suture	GC501945	FDA UDI	Class II	Active
Zcore Form	ZF100	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150ANL-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150AS-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PD-N-2	FDA UDI	Class II	Active
Zcore™ Expand	ZXSINUSS	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes	TXT2530	FDA UDI	Class II	Active
X-Gut™ Chromic Gut Suture	GC5016P45	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PD-2	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0528SS	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150XL-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200PD	FDA UDI	Class II	Active
Zcore™ Expand	ZXSOCKET-10	FDA UDI	Class II	Active
Zcore	ZS100	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFB14-5	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0628PERIO	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PP-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150K2-N-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250AP-N-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250ATC-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PS-N-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250K2-2	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFT8	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0518	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PD	FDA UDI	Class II	Unknown
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150XL-N-2	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0528	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150AP-2	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0428	FDA UDI	Class II	Active
Vitala Porcine Derived Collagen Membranes	VIT1010-1	FDA UDI	Class II	Active
Zderm™	ZD2030TK	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.