9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
OWENS BIOPSY FORCEPS
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690114017·PS-R Insert, Size 2 x 24mm
NOVA LITE TM THYROID
FDA 510(k)
FDA Class 2
·Immunology
LIQUICHEK ANTI-SMOOTH MUSCLE CONTROL, POSITIVE, CATALOG #129
FDA 510(k)
FDA Class 2
·Immunology
BI-METRIC HIP LATERALISED FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·March 2, 2017
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 22, 2013
NEXGEN STEMMED TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code HSH·December 7, 2010
OPTISENSE
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014
Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026