RING SIM 700FF33 FULLY FLEXIBLE

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Simulus Flexible Annuloplasty Ring

FDA registration

Medtronic Mexico S. de R.L. de CV·1 product·🇲🇽 Mexico

Simulus Flexible Annuloplasty Ring

FDA registration

Medtronic Heart Valves Division·1 product·🇺🇸 United States

ATS SIMULUS ANNULOPLASTY RING, MODEL 700FF

FDA 510(k)

FDA Class 2 ·Cardiovascular

Ring, Annuloplasty

FDA classification

FDA Class 2 ·Ring, Annuloplasty

Reprocessed External Fixation Device

FDA registration

Stryker Sustainability Solutions·3 products·🇺🇸 United States

Tri-Plus Encompass Press-Fit Hip Stem

FDA registration

ORTHO DEVELOPMENT CORP.·2 products·🇺🇸 United States

Reprocessed External Fixation Device

FDA registration

Stryker Sustainability Solutions Phoenix·3 products·🇺🇸 United States

Ortho1399 (SN,EP1) - Press-fit Hip System: Encompass Hip Stem

FDA registration

ISOMEDIX OPERATIONS INC·2 products·🇺🇸 United States

Encompass Plasma Sprayed, Press-fit Hip System: Encompass Hip Stem, Tri-plus Acetabular Shell, Tri-plus DCM Liner

FDA registration

ORCHID UNIQUE·2 products·🇺🇸 United States

Ortho1399 (SN,EP1) - Press-fit Hip System: Encompass Hip Stem

FDA registration

ISOMEDIX OPERATIONS INC.·2 products·🇺🇸 United States

Mendell

FDA registration

Mendell·2 products·🇺🇸 United States

INSTRU-MED TECHNOLOGIES

FDA registration

INSTRU-MED TECHNOLOGIES·2 products·🇺🇸 United States

appliance, fixation, nail/blade/plate combination, multiple component Reprocessed External Fixation Devices

FDA registration

Sterigenics US LLC·3 products·🇺🇸 United States

StrykerSustainability (SDA) - Reprocessed External Fixation Devices

FDA registration

Isomedix Operations Inc.·3 products·🇺🇸 United States

Synergy Health Sterilisation UK Ltd

FDA registration

Synergy Health Sterilisation UK Ltd·1 product·🇬🇧 United Kingdom

BAYLIS PAIN MANAGEMENT GENERATOR MODEL: PMG-115 (FOR DOMESTIC USE), PMG-230 (FOR INTERNATIONAL USE)

FDA 510(k)

FDA Class 2 ·Neurology

SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE

FDA 510(k)

FDA Class 2 ·Microbiology

Generator, Lesion, Radiofrequency

FDA classification

FDA Class 2 ·Generator, Lesion, Radiofrequency

Manual Antimicrobial Susceptibility Test Systems

FDA classification

FDA Class 2 ·Manual Antimicrobial Susceptibility Test Systems