10 results
·
17ms
·
Sources: EU EUDAMED, US FDA
G.E. STERILE BREAST BIOPSY/LOCALIZATION TRAY
FDA 510(k)
FDA Class 2
·General Hospital
Peerless Buccal Tube
FDA UDI
ORMCO CORPORATION·00889989023008·PRLS 10 UFM COMBI B/T -10TRQ 22X45 RT
iNSitu™ Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127023835·Starter Rasp
Guided Spade Drill
FDA UDI
BICON, LLC·00813110026613·6.0mm Guided Spade Drill
X-RAY SCANNER, COMPUTERIZED TOMOGRAPHIC
FDA 510(k)
FDA Class 2
·Radiology
OLYMPUS RF LATEX CALIBRATOR, AND OLYMPUS RF LATEX REAGENT WITH MODEL(S): ODC0028, AND OSR61105.
FDA 510(k)
FDA Class 2
·Immunology
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 14, 2013
EON MINI
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 23, 2014
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·January 13, 2011
CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026