CranioFit

FDA registration

BIOPLATE, INC.·1 product·🇺🇸 United States

PEEK Patient Specific Cranial/Craniofacial Implant(PSCI)

FDA registration

KONTOUR (XI'AN) MEDICAL TECHNOLOGY CO., LTD.·1 product·🇨🇳 China

PEEK Patient Specific Cranial/Craniofacial Implant(PSCI)

FDA 510(k)

FDA Class 2 ·Neurology

Plate, Cranioplasty, Preformed, Non-Alterable

FDA classification

FDA Class 2 ·Plate, Cranioplasty, Preformed, Non-Alterable

NA

FDA UDI

DEPUY MITEK, LLC·10886705003501·REUSABLE OBTURATOR 5.5 x 90mm

PMT® Halo Systems

FDA UDI

PMT CORPORATION·00650551114420·HALO, CTLSO VEST SMALL, COOLMAX LINER, 1211-1 X...

OsseoShaper 2

FDA registration

NOBEL BIOCARE DISTRIBUTION CENTER BV·4 products·🇳🇱 Netherlands

N1 TiUltra TCC Implant System

FDA registration

Toothsmiths Incorporated·4 products·🇺🇸 United States

Abutment Screw Retrieval Instrument

FDA registration

MICRO PRECISION SWISS·4 products·🇺🇸 United States

OsseoShaper 2

FDA registration

Nobel Biocare Services AG·4 products·🇨🇭 Switzerland

visor2 system

FDA registration

EEMAGINE MEDICAL IMAGING SOLUTIONS GMBH·4 products·🇩🇪 Germany

Rescue Drill Guide Trioval Conical Connection

FDA registration

ELOS MEDTECH PINOL A/S·1 product·🇩🇰 Denmark

OsseoShaper 2

FDA registration

NOBEL BIOCARE AB, PRODUKTION·4 products·🇸🇪 Sweden

OsseoShaper 2

FDA registration

NOBEL BIOCARE AB·4 products·🇸🇪 Sweden

Synergy Health Ede BV

FDA registration

Synergy Health Ede BV·4 products·🇳🇱 Netherlands

ALEUTIAN® Interbody Systems

FDA UDI

K2M, INC.·10888857522336·Trial Size 13x16x6 mm, 15°

ANCHOR BOLT NUT

FDA UDI

Biomet Orthopedics, LLC·00887868024139·

visor2 system

FDA 510(k)

FDA Class 2 ·Neurology

IN-TIME RETRIEVAL DEVICE

FDA 510(k)

FDA Class 2 ·Cardiovascular

Device, Percutaneous Retrieval

FDA classification

FDA Class 2 ·Device, Percutaneous Retrieval