10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BIPOLAR HF CABLE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROXIMATE ILS CIRCULAR STAPLES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.·Product code GAG·June 7, 2006
TIBIAL NAIL, STANDARD 10X390 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·March 17, 2010
Rotium Bioresorbable Wick
FDA 510(k)
FDA Class 2
·Orthopedic
CEFAR DUAL
FDA 510(k)
FDA Class 2
·Neurology
PROXIMATE ILS CIRCULAR STAPLERS
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.·Product code GAG·June 7, 2006
DEPUY ASR XL FEM IMP SIZE 45
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 28, 2013
ASR ACETABULAR CUPS 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 31, 2011
LC PCA NEW 802.11 AB
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code MEA·July 3, 2014
BV Pulsera with Software Release 2.3-A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718095
FDA Enforcement
Class II
·Ongoing·Philips North America Llc·December 15, 2021