62 results · 24ms · 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.

VenSure Balloon Device, VenSure Nav Balloon Device

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

16PW - Washington Gas - Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588014425·16PW - Washington Gas - Poly White

MULTIFIT TOTAL HIP SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

HMS-DHR-3 NEUROMUSCULAR STIMULATOR

FDA 510(k)
FDA Class 2 ·Physical Medicine

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 31, 2025

INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·November 12, 2014

6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, PUERTO RICO, B.V.·Product code MGB·October 16, 2008

ARDIS PEEK IMPLANT 08X09X22

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code MAX·August 3, 2011

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013

BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 40 SIZE S

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 2, 2024

STEM: M-VIZION DISTAL STEM Ø14MM L 180MM STRAIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 9, 2023

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 3, 2025

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 2, 2025

MECTACER BIOLOX DELTA FEMORAL BALL HEAD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 25, 2025

STEM: M-VIZION DISTAL STEM Ø13MM L 140MM STRAIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 25, 2024

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 29, 2025

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 19, 2024

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·May 30, 2025

RF MARINR

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code LPB·October 1, 2015

EXCOR BLOOD PUMP PU VALVES 10 ML, IN/OUT 6 MM

FDA Adverse Event
Malfunction ·BERLIN HEART GMBH·Product code DSQ·July 14, 2014