SJM Confirm Implantable Cardiac Monitor, Model DM2100

FDA registration

ABBOTT MEDICAL·3 products·🇺🇸 United States

SJM Confirm Implantable Cardiac Monitor, Model DM2100

FDA registration

Abbott Medical·3 products·🇺🇸 United States

SJM CONFIRM IMPLANTABLE CARDIAC MONITOR

FDA 510(k)

FDA Class 2 ·Cardiovascular

Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)

FDA classification

FDA Class 2 ·Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)

ArgenZ HT+ 98x22 OM2

FDA UDI

ARGEN CORPORATION, THE·D818122090·Dental porcelain/ceramic restoration kit

Ceramco®

FDA UDI

Dentsply International Inc.·D0011220900·

Forestanit®

FDA UDI

Forestadent Bernhard Förster GmbH·EFOR21220901·Forestanit wire round hard laboratory coil 0,90 mm

16PW - Class A 21 Lawson - Poly White

FDA UDI

Certified Safety Manufacturing, Inc.·00766588620909·16PW - Class A 21 Lawson - Poly White

Intervertebral fusion device with integrated fixation, lumbar

FDA registration

SpineSmith Holdings, LLC·1 product·🇺🇸 United States

Integra

FDA registration

INTEGRA LIFESCIENCES CORPORATION·1 product·🇺🇸 United States

SURGICAL INSTRUMENT MANUFACTURERS, LLC

FDA registration

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

Bahadir Rigid Lite Sterile Container Systems

FDA registration

BAHADIR USA LLC·1 product·🇺🇸 United States

Integra

FDA registration

Integra Canada ULC·1 product·🇨🇦 Canada

Spine Smith 0302-1420 VisuALIF: Medium 29mm x 36mm PEEK Implant: 14mm x 20°

FDA registration

BANISTER TOOL, INC.·1 product·🇺🇸 United States

Integra

FDA registration

Integra LifeSciences Corporation·1 product·🇺🇸 United States

CosmoLock Pedicle Screw System

FDA UDI

Kalitec Direct LLC·B07311K1220100·Breaker, Extended Tab

Catheter Introducer

FDA registration

Nypro Inc (Maple Grove)·2 products·🇺🇸 United States

SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

SYNTEX PRE-POWDERED NITRILE EXAMINATION GLOVE

FDA 510(k)

FDA Class 1 ·General Hospital

Intervertebral Fusion Device With Integrated Fixation, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Lumbar