71 results · 27ms · Sources: EU EUDAMED, US FDA

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Photoelectric Therapy System

FDA 510(k)
FDA Class 2 ·Radiology

Epimed

FDA UDI
EPIMED INTERNATIONAL, INC·00818788020505·20g TW x 8.0" Coudé® Blunt Nerve Block Needle w...

External Fixation

FDA UDI
Life Spine, Inc.·00190837034153·Protective Cap

Ophthalmic Ring

FDA UDI
KATENA PRODUCTS, INC.·00841668100813·FLIERINGA FIXATION RING 20MM

NORMOFLO IRRIGATION FLUID WARMER, MODELS H-1100, H-1129, NORMOFLO IRRIGATION WARMING SET, MODELS, IR-40, IR-500, IR-600,

FDA 510(k)
FDA Class 2 ·General Hospital

DEPUY RECLAIM REVISION HIP SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HTQ·July 24, 2023

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY IRELAND - 3015516266·Product code HTQ·February 26, 2024

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HTQ·October 7, 2024

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HTQ·June 20, 2023

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY IRELAND - 9616671·Product code HTQ·October 21, 2024

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HTQ·January 24, 2022

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY CMW - 9610921·Product code LOD·November 1, 2019

ABBOTT FREE STYLE LIBRE-3 DIABETIC SENSOR

FDA Adverse Event
Injury ·ABBOTT DIABETES CARE INC.·Product code QBJ·March 20, 2026

ABBOTT FREE STYLE LIBRE-3 DIABETIC SENSOR

FDA Adverse Event
Injury ·ABBOTT DIABETES CARE INC.·Product code QBJ·March 20, 2026

S-ROM*SLEEVE PRX ZTT, 18D-LRG

FDA Adverse Event
Injury ·9616671 DEPUY IRELAND·Product code LPH·October 22, 2013

ABBOTT FREE STYLE LIBRE-3 DIABETIC SENSOR

FDA Adverse Event
Injury ·ABBOTT DIABETES CARE INC.·Product code QBJ·March 20, 2026

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LOD·July 8, 2020

VMP ENDURANCE 80G

FDA Adverse Event
Malfunction ·DEPUY IRELAND - 3015516266·Product code LOD·April 10, 2025

UNKNOWN KNEE INSTRUMENT

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LXH·July 11, 2019