33 results
·
22ms
·
Sources: EU EUDAMED, US FDA
RF-Relief
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869642477·MOSS Ti Pedicle Screw, Ø10.0x95mm DL, polyaxial...
Sochi
FDA UDI
Altus Spine, LLC·00843210173696·Pre-Curved Rod, 3.5mm x 95mm
DIRECT PERORAL CHOLANGIOSCOPY BALLOON
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PROLITE III TOWER AND PR AND HR HANDPIECE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
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
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
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 20, 2025
GMK PRIMARY TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·March 10, 2026
SCRDRIVERSHAFT-CRUCIF 2.4 L100
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·June 20, 2013
NDEHP 2CLV YSTE MICR
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·July 7, 2011
ULTRAFLEX COVERED NG ESOPHAGEAL STENT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code ESW·September 29, 2008
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024