79 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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M SEIRES PATIENT MONITOR MODEL M66, M69, M8000, M9000, M7000
FDA 510(k)
FDA Class 2
·Cardiovascular
Zavation
FDA UDI
Zavation LLC·00842166183704·RASP, 8mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694001373·10mm Chin Plate
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 46mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665037135·
Adult BP Cuff (standard) 24-32cm
FDA UDI
VASOMEDICAL, INC.·00817980020658·Adult BP Cuff (standard) 24-32cm
SAVANNAH
FDA UDI
SPINAL ELEMENTS·00840916151508·SAVANNAH®-T ROD REDUCER SHAFT OUTER SHAFT ASSE...
SAVANNAH
FDA UDI
SPINAL ELEMENTS·00840916151522·SAVANNAH®-T ROD REDUCER - MEASURE
SAVANNAH
FDA UDI
SPINAL ELEMENTS·00840916151492·SAVANNAH® -T ROD REDUCER BACK ASSEMBLY
SAVANNAH
FDA UDI
SPINAL ELEMENTS·00840916151515·SAVANNAH®-T ROD REDUCER SHAFT INNER SHAFT
SAVANNAH
FDA UDI
SPINAL ELEMENTS·00840916151539·SAVANNAH®-T ROD REDUCER T-HANDLE T-HANDLE BACK...
KNIGHT ENDOSCOPIC SPINE SYSTEM (KESS)
FDA 510(k)
FDA Class 2
·Orthopedic
NUVOLASE 532 MEDICAL LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OsteoMed
FDA UDI
OSTEOMED LLC·00845694063173·2.0 System 10mm Chin Plate Sterile Qty 2
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·ATRICURE SYNERGY ABLATION SYSTEM
RD SET YI
FDA Adverse Event
Malfunction
·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021
RD SET DCI
FDA Adverse Event
Malfunction
·MASIMO - 15750 ALTON PKWY·Product code DQA·February 10, 2023
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·Synergy Ablation System
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·ATRICURE SYNERGY ABLATION SYSTEM
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·AtriCure Isolator Clamp, AtriCure Long Clamp, AtriCure Synergy Clamp
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·Synergy Ablation System