MEDPOR CONTAIN CAN Implant

FDA registration

STRYKER LEIBINGER GMBH & CO. KG·1 product·🇩🇪 Germany

MEDPOR CONTAIN Implant

FDA registration

STRYKER LEIBINGER GMBH & CO. KG·1 product·🇩🇪 Germany

GUIDOR ES Membrane

FDA registration

Collagen Matrix, Inc·1 product·🇺🇸 United States

NEOSS AB

FDA registration

NEOSS AB·1 product·🇸🇪 Sweden

Sterigenics U.S., LLC

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Cytoflex Ti-Enforced Membrane

FDA registration

UNICARE BIOMEDICAL, INC.·1 product·🇺🇸 United States

MembraGel

FDA registration

INSTITUT STRAUMANN AG·1 product·🇨🇭 Switzerland

Gammatom S.r.l.

FDA registration

Gammatom S.r.l.·1 product·🇮🇹 Italy

WESLEY COE (CAMBRIDGE) LTD

FDA registration

WESLEY COE (CAMBRIDGE) LTD·1 product·🇬🇧 United Kingdom

Opentex

FDA registration

HANSAmed Limited DBA Citagenix·1 product·🇨🇦 Canada

MICRO/MINI N-PK(H) BONE ANCHOR

FDA 510(k)

FDA Class 2 ·Orthopedic

MICRO/MINI N-PK(F) BONE ANCHOR

FDA 510(k)

FDA Class 2 ·Orthopedic

RPM Reinforced PTFE Mesh

FDA registration

OSTEOGENICS BIOMEDICAL, INC.·2 products·🇺🇸 United States

dental bone plate

FDA registration

Steritec Services, LLC·2 products·🇺🇸 United States

Cytoplast™ Titanium-Reinforced PTFE Membranes

FDA UDI

Osteogenics Biomedical Inc·D765TI150ATCN10·Non-resorbable Textured PTFE Barrier Membrane, ...

RPM™ Reinforced PTFE Mesh

FDA UDI

Osteogenics Biomedical Inc·D765RPM250PDML0·RPM™ Reinforced PTFE Mesh is a temporarily impl...

GUIDOR

FDA UDI

SUNSTAR AMERICAS, INC.·00070942000062·GUIDOR® Bioresorbable Matrix Barrier

GUIDOR

FDA UDI

SUNSTAR AMERICAS, INC.·00070942000017·GUIDOR® Bioresorbable Matrix Barrier

Cytoplast™ Titanium-Reinforced PTFE Membranes

FDA UDI

Osteogenics Biomedical Inc·D765TI250PDN20·Non-resorbable Textured PTFE Barrier Membrane, ...

OpenTex

FDA UDI

PURGO BIOLOGICS Inc.·08800039000918·