16 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ERCHONIA VERJU LASER SYSTEM WITH MASSAGER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16711309220·
A.S.A.P. All Surface Access Polishers Indirect+ Intraoral Point Adjuster
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172015776·Dental abrasive point, re-usable
A.S.A.P.® All Surface Access Polishers Indirect+ Intraoral Point Adjuster Refill
FDA UDI
DEN-MAT HOLDINGS, LLC·00359883004361·Dental abrasive point, re-usable
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P13092270·13mm PLIF Implant 9mm Wide 22mm Length, 7 deg L...
ZEUS-P
FDA UDI
SPINAL ELEMENTS·00840916153366·Zeus-P Trial, 13 x 9 x 22mm
Ardis®
FDA UDI
ZIMMER SPINE, INC.·00889024333840·
Ardis®
FDA UDI
ZIMMER SPINE, INC.·00889024334571·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1671001309220·
OLYMPUS EMPOWER H65
FDA Adverse Event
Malfunction
·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022
VIVASENS
FDA 510(k)
FDA Class 2
·Dental
PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 28, 2025
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 24, 2013
PUMP, INFUSION, IMPLANTED, PROGRAMMABLE
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·September 30, 2014
REVEAL XT
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DSI·June 16, 2011