10 results
·
23ms
·
Sources: EU EUDAMED, US FDA
HyperFlex® Bunion Correction System
FDA 510(k)
FDA Class 2
·Orthopedic
N/A
FDA UDI
Scientific Device Laboratory, Inc.·00810047421658·TB Splashproof Container No rack - (2 1000 ml b...
Surgical Mask
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ZIMMER DENTAL ONE-PIECE IMPLANT
FDA 510(k)
FDA Class 2
·Dental
IMP,1-PC,ANG,3.0X13MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·September 19, 2024
IMP,1-PC,ANG,3.0X13MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·October 11, 2019
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 12, 2014
ILAB ULTRASOUND IMAGING SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (CE)·Product code OBJ·July 29, 2013
S-ICD SYSTEM
FDA Adverse Event
Malfunction
·CAMERON HEALTH·Product code LWS·November 27, 2015
X25 FINAL TIGHTENER
FDA Adverse Event
Malfunction
·DEPUY SPINE INC·Product code HWR·May 3, 2018