12 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Aintree Intubation Catheter, Arndt Airway Exchange Catheter Set, Cook Airway Exchange Catheter, and Cook Airway Exchange Catheter - Extra Firm With Soft Tip
FDA 510(k)
FDA Class 1
·Anesthesiology
SURGISIS RVP RECTO-VAGINAL FISTULA PLUG
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BLEASE700/900 SERIES VENTILATORS
FDA 510(k)
FDA Class 2
·Anesthesiology
MERSILENE POLYESTER FIBER SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAT·September 21, 2020
CAPSURE SP
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 14, 2011
ROTALINK? PLUS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - CORK·Product code MCX·June 11, 2013
PINN MAR +4 NEUT 36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·September 15, 2008
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code HSD·January 9, 2024
EQUINOXE PRESERVE STEM 12MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·May 29, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·July 2, 2019
HEARTMATE 3 VAD MODULAR CABLE
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·August 18, 2022
EQUINOXE REVERSE 46MM GLENOSPHERE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·October 2, 2024