511 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
OMEGA 2 SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481127366·LOCATOR R-Tx Attachment System for BLX, Strauma...
VIDAS® Prolactin
FDA UDI
BIOMERIEUX SA·03573026156961·VIDAS ® Prolactin (PRL) assay is a quantitative...
Curaplex
FDA UDI
BOUND TREE MEDICAL, LLC·00810094579678·Slim Pro-Adult Angulated Size 4A Blade
CONMED
FDA UDI
Conmed Corporation·30653405042444·SADDLEBAG BASKET, Electrosurgical Unit Cart
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481128585·LOCATOR R-Tx Abutment, Straumann BLX, 1 mm
Life Instruments
FDA UDI
Life Instrument Corporation·M930704100100·Surgical Fork
Baby Gorilla®/Gorilla® Plating System
FDA UDI
Paragon 28, Inc.·00889795039668·Hole Counterbore, 3-in-1,TUFFNEK®
MONTANE TAURUS B-S1.F4 [SZER 120 CM]
FDA UDI
MEDEN INMED SP Z O O·05903684802401·The MONTANE treatment table is a treatment tabl...
TEAM-UP TM DENTAL ELECTRONIC ANESTHESIA SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3
FDA 510(k)
FDA Class 2
·Dental
9616026-2006-00240
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
9616026-2006-00244
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
CRE PRO GI
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNQ·May 1, 2025
LIFEPAK CR(R) PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·April 8, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 27, 2014
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 23, 2011
9616026-2006-00239
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
NEPHROMAX KIT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LJE·March 16, 2026
9616026-2006-00222
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006