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 7 of 7

Device	Model / Reference	Registries	Class	Status
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150PLT-1	FDA UDI	Class II	Active
Surgiform® PTFE Suture	CS330S65	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti150BLL-1	FDA UDI	Class II	Active
Cytoplast™ Osteo-Mesh TM-300	TM2534NS	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFB12-5	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PS-2	FDA UDI	Class II	Active
Resorba Suture Sample Pack	KIT001	FDA UDI	N/A	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes	GBR1224	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250PL-1	FDA UDI	Class II	Active
Zcore™ Expand	ZXSINUSL	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFB14	FDA UDI	Class II	Active
Zcore™ Expand	ZXSOCKET	FDA UDI	Class II	Active
Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced	Ti250AP-2	FDA UDI	Class II	Active
RPM™ Reinforced PTFE Mesh	RPM200PST	FDA UDI	Class II	Active
Pro-fix™ Precision Fixation System	PFDB	FDA UDI	Class I	Active
X-Gut™ Chromic Gut Suture	GC401945	FDA UDI	Class II	Active
Zcore Form	ZF050	FDA UDI	Class II	Active
X-Gut™ Plain Gut Suture	GP301945	FDA UDI	Class II	Active
Immix Bone Graft Extender	K013764	FDA 510(k)	Class II	Active
Cytoplast Resorb, Models R-250, Rp-250, Ru-250, Rps-250, Rpl-250	K993610	FDA 510(k)	Class II	Active
Cytoplast Ptfe Suture	K072076	FDA 510(k)	Class II	Active
Pro-Fix Precision Fixation System Model Pfm#, Pfb#, Pft#	K093719	FDA 510(k)	Class II	Active
Osteo-Mesh Tm-300	K984230	FDA 510(k)	Class II	Active
Cytoplast Suture; Cs-0318, Cs-0416, Cs-0418, Cs-0513, Cs-0513pc, Cs-0516hc	K003028	FDA 510(k)	Class II	Active
RPM Reinforced PTFE Mesh	K171774	FDA 510(k)FDA UDI	Class II	Active
Cytoplast Titanium-Reinforced PTFE Membranes	K201187	FDA 510(k)	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.