16 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Ahmed Glaucoma Valve
FDA 510(k)
FDA Class 2
·Ophthalmic
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741620600·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674162060060·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1620600·16mm H x 20mm W x 60mm L x 0 degrees XLIF
Epimed
FDA UDI
EPIMED INTERNATIONAL, INC·00818788020420·20g TW x 6.0" Blunt Nerve Block Needle w/ Intro...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X162060120·16mm H x 20mm W x 60mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L162060120·16mm H x 20mm W x 60mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X16206080·16mm H x 20mm W x 60mm L x 8 degrees XLIF
RADIANCE
FDA 510(k)
FDA Class 2
·Radiology
CLEVER TD-7001NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 24, 2025
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·October 10, 2014
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 11, 2013
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 12, 2011
PEDICLE SCREW LATERAL CONNECTOR L150
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·December 13, 2023
MAGNETOM Verio Dot Upgrade. Model Number: 10684334.
FDA Enforcement
Class I
·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025