10 results
·
32ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Arthrex LoopLoc Knotless Suture
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958001925·600 Micron Disposable Diode Laser Lightguide, 6...
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116022601·Dornier 600 µm Single-Use SMA UroBeam Diode Las...
Cannulated Compression Device System
FDA 510(k)
FDA Class 2
·Orthopedic
XHIBIT CENTRAL STATION, MODEL 96102
FDA 510(k)
FDA Class 2
·Cardiovascular
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 6, 2025
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·July 8, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·October 29, 2014
COULTER® LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·July 8, 2013
iChem VELOCITY Urine Chemistry Strips, REF 800-7212, 100 test strips/vial. The firm name on the label is Beckman Coulter Ireland, Inc., Co. Clare, Ireland, Made in Germany.
FDA Enforcement
Class II
·Terminated·Beckman Coulter Inc.·July 10, 2019