185 results · 22ms · Sources: EU EUDAMED, US FDA

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PREMIER 9000 8 CHANNEL PHASED ARRAY CTL SPINE COIL

FDA 510(k)
FDA Class 2 ·Radiology

Speedlock

FDA UDI
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657042857·Microscissors, Extremely Delicate Tip, Shaft 5m...

Speedlock

FDA UDI
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657023641·Tumor Grasper, 5mm, Blunt End Handle: 1366 Stan...

Speedlock

FDA UDI
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657030687·Speedlock Johan Grasping Forceps, 5

PROSTEC 125I BRANCHYTHERAPY SNAPSEED

FDA 510(k)
FDA Class 2 ·Radiology

CUSTOM TCI-COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

ASR 300 SPIKED CUP SIZE 52

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·April 2, 2013

MG II POROUS TOTAL KNEE SYSTEM PEGGED TIBIA

FDA Adverse Event
Injury ·ZIMMER INC·Product code JWH·March 23, 2011

SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·April 18, 2008

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x37,5 mm Catalog Number: 18965037S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

FDA Enforcement
Class II ·Terminated·Stryker GmbH·June 24, 2020

BD PHOENIX¿ PMIC/ID-107

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 4, 2025