71 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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