30 results
·
23ms
·
Sources: EU EUDAMED, US FDA
EarlySense Central Display Station (CDS)
FDA 510(k)
FDA Class 2
·Cardiovascular
BrightGear Headgear
FDA UDI
ORMCO CORPORATION·00889989079920·PAD,CERVICAL BLACK
AGC Tradition Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304001787·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311510060·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321510060·
Symmetry Hudson
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482000328·Symmetry® Burr; Hudson; 14 mm
NobelProcera®
FDA UDI
Nobel Biocare AB·07332747099584·CYL. FOR MULTI-UNIT NP/RP
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306830822·Instrument ID Tape, Purple, Roll 6.35mm x 762cm
ELMED
FDA UDI
ELMED INCORPORATED·00842180162006·BURR (14MM)
WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
IBOND NEXT GENERATION
FDA 510(k)
FDA Class 2
·Dental
NA
FDA UDI
aap Implantate AG·04042409192203·Cortical Screw 1.5, self-tapping, L 6
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197495776·RZ Rainer Chisel
straig...
ASTRAL 150 - AMER
FDA Adverse Event
Malfunction
·RESMED PTY LTD·Product code NOU·September 18, 2024
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 12, 2025
NA
FDA UDI
aap Implantate AG·04042409192418·Cortical Screw 1.5, self-tapping, L 6
TENACULUM FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·June 6, 2013
UNKNOWN DEPUY FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 30, 2011
GEMSTAR PUMP SET WITH 0.2MICRON FILTER AND PA-ASV
FDA Adverse Event
Malfunction
·HOSPIRA DE COSTA RICA LTD.·Product code FRN·August 28, 2008
PRODIGY AUTOCODE
FDA Adverse Event
Injury
·OK BIOTECH CO., LTD.·Product code NBW·August 4, 2016