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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 4 of 7

Device	Model / Reference	Registries	Class	Status
RPM™ Reinforced PTFE Mesh	RPM200PTC	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS052619	FDA UDI	Class II	Active
X-Gut™ Chromic Gut Suture	GC5013P45	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200PTCM	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PD-N-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFT4-5	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFB12	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	TI150ATC-N-2	FDA UDI	Class II	Active
Cyotplast™ RTM Collagen	RTM3040	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0628PREMSS	FDA UDI	Class II	Active
Zcore Form	ZF200	FDA UDI	Class II	Active
X-Gut™ Chromic Gut Suture	GC3019P75	FDA UDI	Class II	Active
Cyotplast™ RTM Collagen	RTM2030	FDA UDI	Class II	Active
Surgiform® PTFE Suture	CS430S50SS	FDA UDI	Class II	Active
X-Gut™ Plain Gut Suture	GP302475	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250BL-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PS-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250K2-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PS-N-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	TI250ANL-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PP-N-2	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFB8	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0528BK	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFT	FDA UDI	Class I	Active
Cytoplast™ PTFE Suture	CS051819BK	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes	TXT2530-1	FDA UDI	Class II	Active
Zderm™	ZD3040TK	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes	TXT1230	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes	GBR2530	FDA UDI	Class II	Active
Vitala Porcine Derived Collagen Membranes	VIT1520-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0628RC	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PST-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250XL-N-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150BLL-N-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS071816	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250K2-N-2	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PS	FDA UDI	Class II	Unknown
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PP-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PL-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PP-N-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0628PREM	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes	TXT1220-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFT3-5	FDA UDI	Class II	Active
Surgiform® PTFE Suture	CS430R18	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PTC	FDA UDI	Class II	Unknown
Surgiform® PTFE Suture	CS330R24	FDA UDI	Class II	Active
Vitala Porcine Derived Collagen Membranes	VIT2030-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250AS-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PL-1	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250XLK	FDA UDI	Class II	Unknown

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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.