BEACON-S Attenuation Correction option for AXIS and IRIX Nuclear Cameras

FDA registration

PHILIPS MEDICAL SYSTEMS TECHNOLOGIES LTD.·1 product·🇮🇱 Israel

BEACON-S Attenuation Correction option for AXIS and IRIX Nuclear Cameras

FDA registration

Philips Electronics Ltd·1 product·🇨🇦 Canada

BEACON, MODEL 211060

FDA 510(k)

FDA Class 2 ·Radiology

MENISCAL ROOT REPAIR PACK WITH ULTRATAPE SUTURE

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

ACUFEX ENDOBUTTON SYSTEM

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

MENISCAL ROOT REPAIR PACK WITH ULTRATAPE SUTURE

FDA registration

SMITH & NEPHEW INC.·1 product·🇺🇸 United States

MENISCAL ROOT REPAIR PACK WITH ULTRATAPE SUTURE

FDA registration

SMITH & NEPHEW INC.·1 product·🇺🇸 United States

MENISCAL ROOT REPAIR PACK WITH ULTRATAPE SUTURE

FDA registration

Arthrocare Corporation·1 product·🇨🇷 Costa Rica

SV-3+

FDA registration

FUTUREMED AMERICA, INC.·1 product·🇺🇸 United States

Smith&Nephew3754 (NR) - EndoButton Fixation Button, 4mm x 12mm

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

MENISCAL ROOT REPAIR PACK WITH ULTRATAPE SUTURE

FDA registration

SMITH & NEPHEW INC.·1 product·🇺🇸 United States

MENISCAL ROOT REPAIR PACK WITH ULTRATAPE SUTURE

FDA registration

Smith & Nephew, Inc.·1 product·🇺🇸 United States

INTERMEDICS MODEL 431-11 IMPLANT ENDOCARD PAC LEAD

FDA 510(k)

FDA Class 3 ·Cardiovascular

MODIFIED NUMED BALLOON ANGIOGRAPHIC CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

System, Tomography, Computed, Emission

FDA classification

FDA Class 2 ·System, Tomography, Computed, Emission

Catheter, Flow Directed

FDA classification

FDA Class 2 ·Catheter, Flow Directed

Permanent Pacemaker Electrode

FDA classification

FDA Class 3 ·Permanent Pacemaker Electrode