8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
SURGITEK PERCUTANEOUS NEPHROSTOMY CATH
FDA 510(k)
FDA Unclassified
·Unknown
MONDEAL
FDA UDI
MONDEAL Medical Systems GmbH·04050435061936·MCD Screw 3.0 x 26 mm cannulated M2
grey
THOR DDII 830CL3 LASER SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
Integrity-SI® Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
ENVISTA INTRAOCULAR LENS
FDA Adverse Event
Injury
·BAUSCH & LOMB·Product code HQL·May 1, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·November 13, 2012
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV·Product code FNL·September 2, 2010
ACCOLADE SR SL MRI (Model L310)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025