16 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Fighter Guidewire, Marvel Guidewire, Samurai Guidewire, Samurai RC Guidewire, Stretch Extension Wire
FDA 510(k)
FDA Class 2
·Cardiovascular
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741518400·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674151840060·
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304674929·
LoFric® Primo™
FDA UDI
Wellspect AB·07333387043210·Single Use Urinary Catheter LoFric Primo Coudé ...
LoFric® Primo™
FDA UDI
Wellspect AB·07392532131585·Single Use Urinary Catheter LoFric Primo Coudé ...
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100257·CHU ASPIRATING SPECULUM SOLID
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587C15184040·15mm H x 18mm W x 40mm L x 4 degree XLIF Corona...
ENSITE VERISMO SOFTWARE
FDA 510(k)
FDA Class 2
·Radiology
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
FDA 510(k)
FDA Class 1
·General Hospital
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 8, 2014
CARELINK
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code DXY·June 7, 2013
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 6, 2011
CPS SM SHT SPDL W PINS 600LBF
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·August 28, 2024
OSS 5CM TAPERED DIAPH SEGMENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·August 28, 2024
ELEKTA LIMITED Elekta Synergy Platform, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear
FDA Enforcement
Class II
·Ongoing·Elekta, Inc.·December 13, 2023