79 results · 21ms · Sources: EU EUDAMED, 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