11 results
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29ms
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Sources: EU EUDAMED, US FDA
FLEXIBLE GRASPING FORCEPS
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209126026·
Wildlife
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746031571·ELASTICS INTRA-ORAL MEDIUM 4.5 OZ 1/4" 1000/BAG
Shoreline ACS
FDA UDI
Seaspine Orthopedics Corporation·10889981125387·4.0mm Fixed Angle Screw, Self Tapping, 12mm
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575223664·Femoral component, uncemented, CoCrMo, UHMWPE, ...
Dia-X Sil Bite
FDA 510(k)
FDA Class 2
·Dental
MYOPACH ULTRASONIC PACHOMETER
FDA 510(k)
FDA Class 2
·Radiology
KINETRA
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code MFR·June 6, 2014
ECHELON*FLEX60 ARTICULATING
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 3, 2012
PIONEER PLUS CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC CARDIOVASCULAR·Product code DQY·September 2, 2010
BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026