15 results · 20ms · Sources: EU EUDAMED, US FDA

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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