INTERLOK / HA COPELAND RESURFACING HEADS

FDA registration

BIOMET, INC.·2 products·🇺🇸 United States

INTERLOK / HA COPELAND RESURFACING HEADS

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

FDA classification

FDA Class 2 ·Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

Zirlux

FDA UDI

HENRY SCHEIN, INC.·H65890106350·Zirlux Titanium Esthetic Abutment Posterior com...

DeRoyal

FDA UDI

DEROYAL INDUSTRIES, INC.·00749756185912·ORTHO EXTREMITY TRAY

BV Pulsera

FDA registration

Philips India Limited·3 products·🇮🇳 India

Philips Pulsera C-arm

FDA registration

BAY SHORE MEDICAL EQUIPMENT, LLC·3 products·🇺🇸 United States

Philips Pulsera

FDA registration

CANUTE INTERNATIONAL MEDICAL SERVICES (CANADA) INC·3 products·🇨🇦 Canada

BV Pulsera

FDA registration

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·3 products·🇳🇱 Netherlands

BV Pulsera

FDA registration

Philips India Limited - Image Guided Therapy Systems Business Unit·3 products·🇮🇳 India

PHILIPS BV PULSERA

FDA registration

EvERX PTY LTD·3 products·🇦🇺 Australia

PHILIPS BV PULSERA/ENDURA

FDA registration

CAN TECHNOMED TRADING LTD.·3 products·🇨🇦 Canada

Slendertone Flex Type 512

FDA registration

CHINA TURNKEY SOLUTIONS LOGISTICS (SHENZHEN) CO., LTD.·1 product·🇨🇳 China

CORINNE MCCORMACK INC.

FDA UDI

FGX INTERNATIONAL INC.·00193033185421·

InTess Lumbar Cage

FDA UDI

Kalitec Direct LLC·B07312K0106150·Trial, 26 x 15mm, 8 Degree, Tapered, Straight

CORINNE MCCORMACK INC.

FDA UDI

FGX INTERNATIONAL INC.·00193033185438·

MODIFICATION TO MILLER/GALANTE PRECOAT UNICOMPARTMENTAL KNEE SYSTEM (8 MM ARTICULAR SURFACE)

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

MODIFICATION TO MILLER/GALANTE PRECOAT UNICOMPARTMENTAL KNEE SYSTEM (8 MM ARTICULAR SURFACE)

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

IVS TUNNELLER

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

MODIFICATION TO HP M2376A DEVICE LINK SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular