9 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
AZUR CX DETACHABLE 18
FDA 510(k)
FDA Class 2
·Cardiovascular
ArgenZ ST 98x12 ML OM1
FDA UDI
ARGEN CORPORATION, THE·D818123384·Dental porcelain/ceramic restoration kit
LINEAR ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 23, 2024
COOPERSURGICAL TRIAL TRANSFER CATHETER
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ESCALADE ACETABULAR CUP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 14, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 20, 2008
CAPNOCHECK BCI Airway Adapter; Model Number BSR; Product Code WW1100
FDA Enforcement
Class II
·Ongoing·Smiths Medical ASD, Inc.·March 26, 2025