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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 1 of 7

Device	Model / Reference	Registries	Class	Status
Cytoplast™ PTFE Suture	CS0523	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150XL-N-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0618PREM	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250ANL-N-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250BL-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFMF5-5	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250BL-N-2	FDA UDI	Class II	Active
Vitala Porcine Derived Collagen Membranes	VIT3040-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250XL-N-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PL-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes	TXT1224-1	FDA UDI	Class II	Active
Zcore	ZY050	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250XLK-N-2	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS051819SS	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0618RC	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0618PERIO	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0428SS	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150BL-N-2	FDA UDI	Class II	Active
Surgiform® PTFE Suture	CS430S50	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200XL	FDA UDI	Class II	Active
Cyotplast™ RTMTape	RTMTAPE10	FDA UDI	U	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PST-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFDB56	FDA UDI	Class I	Active
Cytoplast™ PTFE Suture	CS0528BKSS	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFB10	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PLT-N-2	FDA UDI	Class II	Active
Zcore	ZL100	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200PDML	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PD-1	FDA UDI	Class II	Active
Ridge Preservation Kit - Cytoplast Technique	KITRPCT	FDA UDI	N/A	Active
Pro-fix™ Precision Fixation System	PFDH	FDA UDI	Class I	Active
Cytoplast™ PTFE Suture	CS0618PERIOSS	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PL-N-1	FDA UDI	Class II	Active
Surgiform® PTFE Suture	CS330S65SS	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	TI250ANL-N-2	FDA UDI	Class II	Active
X-Gut™ Plain Gut Suture	GP401975	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS052819SS	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PST-N-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PD-N-2	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFT8-5	FDA UDI	Class II	Active
Cytoplast Rtm Collagen	RTM2030-1	FDA UDI	Class II	Unknown
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250K2-N-1	FDA UDI	Class II	Active
Surgiform® PTFE Suture	CS518R13	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200XLKM	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150ANL-2	FDA UDI	Class II	Active
Cyotplast™ RTMFoam	RTMFOAM10	FDA UDI	U	Active
RPM™ Reinforced PTFE Mesh	RPM250PDMR	FDA UDI	Class II	Unknown
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PL-N-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes	TXT1224	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0518K	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.