18 results · 19ms · Sources: EU EUDAMED, US FDA

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Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·PARAPERM O2 CLEAR & BLUE LENS

PressON™

FDA UDI
NEXUS SPINE, L.L.C.·B6788200620·External Pedicle Driver

Monitor, Intracranial Pressure, Implanted

FDA Pre-Market Approval
FDA Class 3 ·COSMAN ICP TELE-SENSOR(R)

Separator, Automated, Blood Cell And Plasma, Therapeutic

FDA Pre-Market Approval
FDA Unclassified ·CRYOMAX(TM)

DISPOSABLE PLASTIC SYRINGE & NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

Monitor, Intracranial Pressure, Implanted

FDA Pre-Market Approval
FDA Class 3 ·COSMAN ICP TELE-SENSOR(R)

Monitor, Intracranial Pressure, Implanted

FDA Pre-Market Approval
FDA Class 3 ·ICP TELE-MONITOR & ICP TELE-SENSOR

Separator, Automated, Blood Cell And Plasma, Therapeutic

FDA Pre-Market Approval
FDA Unclassified ·CRYOMAX(TM)

Separator, Automated, Blood Cell And Plasma, Therapeutic

FDA Pre-Market Approval
FDA Unclassified ·CRYOMAX(TM)

Monitor, Intracranial Pressure, Implanted

FDA Pre-Market Approval
FDA Class 3 ·COSMAN ICP TELE-SENSOR(R) & COSMAN

Monitor, Intracranial Pressure, Implanted

FDA Pre-Market Approval
FDA Class 3 ·COSMAN ICP TELE-SENSOR(R)

Monitor, Intracranial Pressure, Implanted

FDA Pre-Market Approval
FDA Class 3 ·COSMAN ICP TELE-SENSOR(R)

3.5MM LCP® PROXIMAL HUMERUS PLATE-STANDARD 5H SHAFT/114MM

FDA Adverse Event
Injury ·SYNTHES USA·Product code KTW·May 20, 2014

NON AC-POWERED PATIENT LIFT

FDA Adverse Event
Malfunction ·INVACARE SUZHOU·Product code FSA·November 5, 2012

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 23, 2010

BINAXNOW STREP PNEUMONIAE 12T

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025

BINAXNOW STREP PNEUMONIAE 12T

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025

BINAXNOW STREP PNEUMONIAE 12T

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025