15 results
·
20ms
·
Sources: EU EUDAMED, US FDA
INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Mini-Mono®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70603021·Mini-Mono-Brackets Alexander 'S' .022" 20 Brack...
“Paonan” Orthopedic Manual Surgical Instrument (Non-Sterile)
FDA UDI
Paonan Biotech Co.,Ltd.·04719878786911·Curved Probe
Rumor
FDA UDI
Ortho Organizers, Inc.·00190707003678·Rumor .018 UR2 8T 9A 0O
Life Instruments
FDA UDI
Life Instrument Corporation·M930706030200·Bone Funnel Cup
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0600020·Tray Insert, Level 2
VANGUARD COMPLETE KNEE CRUCIATE RETAINING POROUS & HA FEMUR LEFT 75MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code MBH·December 16, 2016
HBS HEADLESS BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
HARDY DISK, PENICILLIN, 10 UNITS
FDA 510(k)
FDA Class 2
·Microbiology
ROSA Straight Cup Inserter Shaft
FDA UDI
Orthosoft Inc·00887868518539·
CONFIDENCE KIT, NO NEEDLES
FDA Adverse Event
Malfunction
·DEPUY SYNTHES SPINE·Product code NDN·April 1, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 11, 2013
PLUM A+ PUMP REFURB
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·August 8, 2014
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 15, 2011
PROXIMATE*HCS HEMORR CIR STAPL
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 5, 2019