42 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PowerPAK Syringe
FDA 510(k)
FDA Class 2
·General Hospital
HeyGears
FDA UDI
Keystone Industries·H66842201141·KeySplint Hard for HeyGears, 1 kg
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112830·BARRON VACUUM PUNCH 9.5MM
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220114150·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220114070·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220114000·
3D KNEE
FDA 510(k)
FDA Class 2
·Orthopedic
Astroglide Organix Liquid
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Widex
FDA UDI
Widex A/S·05706069914665·WIDEX MOMENT MRB2D (Honey blond ) 220, Telecoil...
ONE TOUCH BASIC ENHANCED
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·February 26, 2002
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 25, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 3, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 19, 2025
VERSACROSS CONNECT LAAC ACCESS SOLUTION
FDA Adverse Event
Injury
·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 21, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 12, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 26, 2024