26 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MAXLOCK EXTREME ELBOW FRACTURE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Tasso+
FDA UDI
Tasso Inc.·00850038691004·
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221037107·Unitek(TM) Bicuspid Band General Purpose Wide U...
eTRAX™ Needle
FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436103275·Sterile needle, 14GA x 13cm with (7.6 tapered t...
K2M General Instruments
FDA UDI
VB Spine LLC·10888857580763·Split Tube Retractor Ø20x30 mm
LIMITORR VOLUME LIMITING EVD 20 ML
FDA Adverse Event
Malfunction
·INTEGRA NEUROSCIENCES PR·Product code JXG·June 1, 2015
INSTINCT JAVA SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
STALIF MIDLINE
FDA 510(k)
FDA Class 2
·Orthopedic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149025·Straight Implant Trial 30mm x 11mm x 9mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149094·Straight Implant Trial 30mm x 11mm x 16mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149087·Straight Implant Trial 30mm x 11mm x 15mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149063·Straight Implant Trial 30mm x 11mm x 13mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149049·Straight Implant Trial 30mm x 11mm x 11mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149056·Straight Implant Trial 30mm x 11mm x12mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149018·Straight Implant Trial 30mm x 11mm x 8mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149070·Straight Implant Trial 30mm x 11mm x 14mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149032·Straight Implant Trial 30mm x 11mm x 10mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149001·Straight Implant Trial 30mm x 11m x 7mm
UNKNOWN VLOC PRODUCT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAM·January 31, 2017
PURGE CASSETTE GEN 2, STERILE, NON QSK
FDA Adverse Event
Malfunction
·ABIOMED, INC.·Product code OZD·January 6, 2026