20 results
·
22ms
·
Sources: EU EUDAMED, US FDA
RadPRO® Mobile 40kW; RadPRO® Mobile 40kW FLEXPLUS, Model SM-40HF-B-D-VIR
FDA 510(k)
FDA Class 2
·Radiology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517731364·CoRoent XL+, 13x18x45mm 15°
CoRoent
FDA UDI
Nuvasive, Inc.·00887517638434·CoRoent Ant TLIF PEEK, 16x11x34mm 15°
Symmetry Rochester Ochsner
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482056257·Symmetry® Forceps, Rochester-Oschner, Curved, 1...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694047203·PrimaLIF LLIF PEEK Implant, 13mm X 22mm X 45mm,...
MODIFICATION TO ENDIUS ATAVI SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
WEBSTER CS CATHETER WITH EZ STEER TECHNOLOGY, WEBSTER CS CATHETER WITH EZ STEER TECHNOLOGY AND AUTO ID MODEL: D-1263-04,
FDA 510(k)
FDA Class 2
·Cardiovascular
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013
VISIONAIRE GII FEMOR
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·July 13, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Death
·CORDIS DE MEXICO·Product code NIQ·September 12, 2008
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·December 28, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·November 18, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·November 21, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·November 21, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·November 21, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·November 21, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·December 28, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·November 21, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·November 21, 2025
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·ACUMED, LLC·Product code HRS·November 21, 2025