40 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ARCHER SUPER STIFF GUIDEWIRES
FDA 510(k)
FDA Class 2
·Cardiovascular
JOBST Bella Lite
FDA UDI
BSN MEDICAL, INC.·00035664013394·BELLA LITE 20-30 MM HG ARMSLEEVE LARGE-LONG BRO...
Clean-Bor Tube 2"ID x 39"
FDA UDI
Vacumed·00850644007862·Clean-Bor Tube
Sklar®
FDA UDI
SKLAR CORPORATION·10649111313608·POSILOCK INSTR STRING 18 X 2.5
Astra Vr
FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436111294·ASTRA VR Endovaginal/Endorectal Probe Reprocessor
Indus
FDA UDI
SPINEFRONTIER, INC.·00190361035510·Indus Invue MAX Symmetrical ACP, 2 Level, 39mm
Clean-Bor Tube 2"ID x 39"
FDA UDI
Vacumed·00850644007879·Clean-Bor Tube
OMNILINK ELITE PERIPHERAL STENT SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code NIO·July 22, 2020
QUEST EXERCISE STRESS SYSTEM, MODEL CONFIGURATION 14
FDA 510(k)
FDA Class 2
·Cardiovascular
MRI FASTSYSTEM RETRACTOR SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
AVANTAGE INLAY SIZE 50/28
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code LPH·December 15, 2016
UNKNOWN BIOMET AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017
AVANTAGE E1 INSERT DIA28 S56
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 21, 2016
UNKNOWN BIOMET AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017
G7 BISPHERICAL SHELL 50D
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·December 15, 2025
AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·June 2, 2017
AML SM STATURE 15.0MM
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·May 9, 2013
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014
OT ULTRALINK METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 24, 2011
AVANTAGE UHMWPE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·March 29, 2017