5,955 results · 38ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

GA-E

FDA UDI
AGNES MEDICAL CO., LTD.·08800067700040·

CELT ACD

FDA Adverse Event
Injury ·VASORUM·Product code MGB·May 14, 2026

DIREXION FATHOM-16 SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KRA·October 11, 2024

TRANSEND?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·March 5, 2026

ANGIO-SEAL

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·May 9, 2025

VASSALLO GT FLOPPY

FDA Adverse Event
Malfunction ·FILMECC CO., LTD.·Product code DQX·April 16, 2026

MICRO ACE¿ ADVANCED MICRO ACCESS SYSTEM

FDA Adverse Event
Malfunction ·MERIT MEDICAL SYSTEMS MEXICO·Product code DRE·April 10, 2024

EMBOSPHERE

FDA Adverse Event
Injury ·BIOSPHERE MEDICAL, S.A.·Product code KRD·April 10, 2026

EMBOSPHERE

FDA Adverse Event
Injury ·BIOSPHERE MEDICAL, S.A.·Product code KRD·April 10, 2026

EMBOSPHERE

FDA Adverse Event
Injury ·BIOSPHERE MEDICAL, S.A.·Product code KRD·April 10, 2026

EMBOSPHERE

FDA Adverse Event
Injury ·BIOSPHERE MEDICAL, S.A.·Product code KRD·April 13, 2026

WAVELIGHT EX500 EXCIMER LASER

FDA Adverse Event
Injury ·WAVELIGHT GMBH·Product code LZS·August 5, 2020

GA-B, GA-C, GA-E, GA-I, GA-S, GA-W3A, GA-F3A, GA-IL, GA-SL, GA-W3B, GA-F1A

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

JRNY II CR FEM OX NP LT SZ 3

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·May 29, 2026

VASSALLO GT

FDA Adverse Event
Injury ·FILMECC CO., LTD.·Product code DQX·April 24, 2026

THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

FDA Adverse Event
Death ·THORATEC CORPORATION·Product code DSQ·April 20, 2026

UNKNOWN DEVICE

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code GZF·May 18, 2018

PANOVIEW PLUS

FDA Adverse Event
Injury ·RICHARD WOLF GMBH·Product code HIH·July 10, 2023

6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVICE, US

FDA Adverse Event
Injury ·TERUMO MEDICAL CORPORATION·Product code MGB·May 8, 2024

6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVICE, US

FDA Adverse Event
Injury ·TERUMO MEDICAL CORPORATION·Product code MGB·May 8, 2024