Is this your brand? Sign in to claim ownership.

OSTEOGENICS BIOMEDICAL, INC.

Last updated September 17, 2026

Information

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

Catalogue (326)

Page 5 of 7

Device	Model / Reference	Registries	Class	Status
Cytoplast™ PTFE Suture	CS052819	FDA UDI	Class II	Active
X-Gut™ Chromic Gut Suture	GC3019P45	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PLT	FDA UDI	Class II	Unknown
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PS-N-2	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS0628PERIOSS	FDA UDI	Class II	Active
X-Gut™ Plain Gut Suture	GP302245	FDA UDI	Class II	Active
X-Gut™ Chromic Gut Suture	GC301975	FDA UDI	Class II	Active
Zcore	ZY050	FDA UDI	Class II	Unknown
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PTC-N-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250ANL30-1	FDA UDI	Class II	Active
Cytoplast™ Osteo-Mesh TM-300	TM4545NS	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250BL-N-1	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PST-N-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250BLL-N-2	FDA UDI	Class II	Active
Zcore™ Expand	ZXSOCKET-5	FDA UDI	Class II	Active
Vitala Porcine Derived Collagen Membranes	VIT1325-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150BLL-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PD-N-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS051819	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250ANL30-N-2	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS072816	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250BL	FDA UDI	Class II	Unknown
Zcore	ZL200	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PST	FDA UDI	Class II	Unknown
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PST-N-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFDBCA	FDA UDI	Class I	Active
Cytoplast™ PTFE Suture	CS0518SS	FDA UDI	Class II	Active
Zcore	ZS200	FDA UDI	Class II	Active
Cytoplast™ RTMPlug	RTMPLUG10	FDA UDI	U	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150AP-1	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS052819BK	FDA UDI	Class II	Active
Cytoplast™ PTFE Suture	CS072813SS	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PP-2	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PLT-1	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150XLK-1	FDA UDI	Class II	Active
Cyotplast™ RTM Collagen	RTM1520	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PTC-2	FDA UDI	Class II	Active
X-Gut™ Chromic Gut Suture	GC301945	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM250PLT	FDA UDI	Class II	Unknown
Pro-fix™ Precision Fixation System	PFT10-5	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150BLL-N-2	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti250PTC-N-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFTK10	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200BL	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150ANL-N-2	FDA UDI	Class II	Active
X-Gut™ Chromic Gut Suture	GC4013P45	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150PLT-N-1	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFT4	FDA UDI	Class II	Active
Cytoplast™ Titanium-Reinforced PTFE Membranes	Ti150ATC-N-1	FDA UDI	Class II	Active
Osteo-Mesh Tm-300	TM2534	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.