47 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COGNISION EEG/EP SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
HIGH-WAVE
FDA UDI
Denplus Inc·D8451141316·HIGH-WAVE, ORI, 11.3 kg
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868558832·
Biomet Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304009868·
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515018464·Roch-Pean Hemo Fcps, str, 14" (35.5cm)
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321413160·
K2M General Instruments
FDA UDI
VB Spine LLC·10888857580916·Split Tube Retractor Ø20x80 mm
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973101659·Poly Insert MPCS, Size 3R, 16mm
EDENTA
FDA UDI
EDENTA ETABLISSEMENT·E312C1413160231·Surgical cutters FGXL
ANTIMICROBIAL ALGINATE DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
AAP CANNULATED SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
POSIFLUSH
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 20, 2026
POSIFLUSH
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 1, 2026
BD POSIFLUSH
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026
BD POSIFLUSH
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026
BD POSIFLUSH NORMAL SALINE SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·January 6, 2021
PARIETENE PROGRIP RT PPL/PLA 12X8CM
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code FTL·November 24, 2015
PARIETENE PROGRIP RT PPL/PLA 12X8CM
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code FTL·November 24, 2015
SYRINGE 10ML REG PR SALINE 10ML FILL
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code NGT·August 5, 2021
CAPSURE SP NOVUS
FDA Adverse Event
Death
·MPRI·Product code DTB·June 3, 2013