15 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
HOBBS MEDICAL GRASPING FORCEPS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Stern Root Anchor® Standard Female, Ti
FDA UDI
STERNGOLD DENTAL LLC·00841549106811·The Stern Root AnchorSystem includes the Stern ...
Brasseler USA
FDA UDI
Provision·00810041064912·
Brasseler USA
FDA UDI
Provision·B504OMKM331250·
Reprocessed Oscillating/Sagittal Saw Blade, Thick, 31 x 9 x 0.56mm
FDA UDI
SURETEK MEDICAL·B390KM331251·
Masel
FDA UDI
Ortho Organizers, Inc.·00190707034993·.018 X .025 Upper Elastinol™ Natural Orthocosme...
SMALL BONE BLADES
FDA UDI
Peter Brasseler Holdings, LLC·00887919094234·KM33-125
NA
FDA UDI
STERILMED, INC.·10888551017084·SAW BLADE MICRO OSCILLATING 12 TEETH/CM STRYKE...
Battle Creek Equipment
FDA registration
Battle Creek Equipment·3 products·🇺🇸 United States
WITHINGS BLOOD PRESURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
HANDIVIPP
FDA 510(k)
FDA Class 1
·Physical Medicine
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 17, 2014
NOVASURE IMPEDANCE CONTROLLED EA SYSTEM
FDA Adverse Event
Injury
·HOLOGIC·Product code MNB·November 7, 2012
PAIN CARE 4200
FDA Adverse Event
Injury
·BREG, INC·Product code MEB·September 9, 2010
OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·October 13, 2021