314 results
·
32ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192862·16mm X 100mm Stem Pilot
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916120405·ZEUS®-L Hyper, 14 x 21 x 60mm, 14 Degree
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916134358·ZEUS®-L, Lateral Lumber Interbody Fusion Device...
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916141196·ZEUS® LLIF 14mm x 21mm x 60mm x 21° TRIAL
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916120412·ZEUS®-L, Lateral Lumber Interbody Fusion Device...
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916141127·ZEUS® LLIF 14mm x 21mm x 60mm x 07° TRIAL
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916141165·ZEUS® LLIF 14mm x 21mm x 60mm x 14° TRIAL
STRETCH VINYL EXAMINATION GLOVE POWDER FREE
FDA 510(k)
FDA Class 1
·General Hospital
SONOSURG TROCAR
FDA 510(k)
FDA Unclassified
·Unknown
IMP TM 4.7MM MTX FULL, 11.5MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·November 25, 2022
IMP TM 4.7MM MTX FULL, 10
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026
IMP TM 4.7MM MTX FULL, 10
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 5, 2014
BATHLIFT BLISS RECLINER US AB
FDA Adverse Event
Malfunction
·HANDICARE·Product code FNG·May 23, 2013
PUMP IN STYLE ADVANCED
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·May 26, 2011
IMP TM 4.1MM MTX FULL, 11.5MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·June 1, 2020
IMP TM 4.1MM MTX FULL,10M
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·July 2, 2021
IMP TM 4.7MM MTX FULL, 11.5MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·June 27, 2024
IMP TM 4.7MM MTX FULL, 10
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·July 15, 2024