15 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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POSTERIOR ANNULOPLASTY BAND (MODEL 607)
FDA 510(k)
FDA Class 2
·Cardiovascular
MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·June 11, 2021
DURAN ANCORE RING
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·August 12, 2021
MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·October 26, 2021
MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·May 28, 2022
CG COMPOSITE RING
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·September 2, 2020
DURAN ANCORE RING
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·September 2, 2020
DURAN ANCORE RING
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·July 29, 2021
MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·July 19, 2022
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613084837·K-Wire, Double Ended, Trocar Point, Diameter 0....
Third Eye Panoramic Auxiliary Endoscopy System - Resposable
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CONSERVE PLUS QUADRAFIX ACETABULAR SHELL
FDA 510(k)
FDA Class 3
·Orthopedic
PLUM XLD LTN AMERICA
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·June 23, 2014
VIPER X-25 FINAL TIGHTENER
FDA Adverse Event
Malfunction
·DEPUY SPINE INC.·Product code LXH·December 16, 2010
SIGMA STAB XLK INS 2.5 8MM
FDA Adverse Event
Injury
·9616671 DEPUY (IRELAND)·Product code JWH·February 14, 2013