53 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BIOPSY SCIENCES, INC. HYDROMARK BREST BIOSY SITE MARKER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
K121116
FDA UDI
Life Spine, Inc.·00190837016029·
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837016043·
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837016258·
Premium Tray
FDA UDI
Denplus Inc·D8451121113·Cold-cured acrylic resin, Yellow, 454 g
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690129998·Retaining Bolt, PS or PS-C Insert, Revision Tib...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450474259·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450474655·
PEDICLE SCREW 7X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·April 10, 2018
PEDICLE SCREW 7X50
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·February 23, 2018
PEDICLE SCREW 5X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·March 23, 2018
GUARDIAN II NC HEMOSTASIS VALVE
FDA 510(k)
FDA Class 2
·Cardiovascular
MAMMOPATH
FDA 510(k)
FDA Class 2
·Radiology
M.U.S.T. RODS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·April 20, 2026
PEDICLE SCREW PEDICLE SCREW 5X40
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·January 17, 2024
M.U.S.T. POLYAXIAL PEDICLE SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MNI·October 28, 2024
MUST PEDICLE SCREW 8X40MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2017
PEDICLE SCREW - PEDICLE SCREW 8X75MM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·October 11, 2018
PEDICLE SCREW PEDICLE SCREW 7X45
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·September 9, 2022
MECTALIF OBLIQUE (TI PEEK) INTERBODY FUSION DEVICE 12X28X11 L10
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MAX·April 1, 2020