9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch
FDA 510(k)
FDA Class 2
·Cardiovascular
VITALCONNECT PLATFORM BY VITAL CONNECT INC.
FDA 510(k)
FDA Class 2
·Cardiovascular
GRANDIO CORE DUAL CURE
FDA 510(k)
FDA Class 2
·Dental
CERTAS INLIN VLV SPHN/UNIT CAT
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·January 7, 2022
BD VIPER¿ LT SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code OOI·August 14, 2023
RESTORE PRIME
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 3, 2013
ETS-FLEX - ENDOSCOPIC
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 28, 2011
MAXIM INTRLK TIBIAL PLATE
FDA Adverse Event
Injury
·BIOMET INC.·Product code JWH·September 3, 2008
Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025