SURGICAL INSTRUMENT MANUFACTURERS, LLC

FDA registration

SURGICAL INSTRUMENT MANUFACTURERS, LLC·1 product·🇺🇸 United States

Arena-C HA PEEK Cervical IBFD

FDA registration

Millstone Medical Outsourcing LLC·1 product·🇺🇸 United States

SPINEFRONTIER ARENA-C HA PEEK CERVICAL INTERVERTEBRAL BODY FUSION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04049772814237·GENUMEDI PT SILVER L VI

SeaSpine Spacer System NM

FDA registration

SEASPINE ORTHOPEDICS CORPORATION·2 products·🇺🇸 United States

Millstone Medical Outsourcing LLC

FDA registration

Millstone Medical Outsourcing LLC·2 products·🇺🇸 United States

Prism View

FDA registration

PRISM CLINICAL IMAGING, INC.·2 products·🇺🇸 United States

LEONE SPA

FDA UDI

LEONE SPA·08033707011101·CALIBRA 1ST MOL BANDS W/G8025-02 n.UR 26

OsteoMed

FDA UDI

OSTEOMED LLC·00845694043144·2.0mm, Locking Reconstruction Plate, 5x16 Hole,...

HOSKIN SUTURE FORCEPS

FDA UDI

SONTEC INSTRUMENTS, INC.·00192896073395·HOSKIN SUTURE FORCEPS TITANIUM

Medline ReNewal

FDA registration

Medline ReNewal·1 product·🇺🇸 United States

Sandoz GmbH

FDA registration

Sandoz GmbH·1 product·🇦🇹 Austria

BARD CK PARASTOMAL HERNIA PATCH, MODELS 0118001, 0118002, 0118003, 0118004

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SEASPINE SPACER SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical

Mesh, Surgical, Polymeric

FDA classification

FDA Class 2 ·Mesh, Surgical, Polymeric

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar