9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
WRPAROUND LIMB HOLDER (24446,24446-350,24447-010,24449-010)
FDA 510(k)
FDA Class 1
·General Hospital
ACHIEVA, INTERA AND PANORAMA 1.0T, RELEASE 2.5
FDA 510(k)
FDA Class 2
·Radiology
URESIL OCCLUSION BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
RADIOLUCENT AIMING ARM/FRN GREATER TROCHANTER
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·November 29, 2018
RADIOLUCENT AIMING ARM/FRN GREATER TROCHANTER
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·July 30, 2020
STENOSCOPE
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·December 20, 2010
ADVANTA SST
FDA Adverse Event
Injury
·ATRIUM MEDICAL CORP.·Product code DSY·January 2, 2013
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 29, 2014
CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026