71 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Painless IPL System - KDT750
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526781719·LUMBAMED FACET 3 POINT SILVER IV
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526743670·ACHIMED ACHILLES SUPP SILVER IV
BD Calibrated Disposable Inoculating Loops, Green
FDA UDI
BECTON, DICKINSON AND COMPANY·00382902202141·BD Calibrated Disposable Inoculating Loops, Gre...
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113102·PS Insert, Size 2 x 14mm
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220214000·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220214150·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220214070·
Coral
FDA UDI
Seaspine Orthopedics Corporation·10889981029203·Fixed X-Conn 14mm
TBD
FDA 510(k)
FDA Class 2
·Ophthalmic
MEDIAL ROTATION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEDIAL ROTATION KNEE
FDA Adverse Event
Injury
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROATION KNEE
FDA Adverse Event
Malfunction
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROATION KNEE
FDA Adverse Event
Injury
·MATORHTO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROTATION KNEE
FDA Adverse Event
Malfunction
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROTATION KNEE
FDA Adverse Event
Injury
·MATORTHO LIMITED·Product code JWH·January 22, 2016
VERSACROSS CONNECT LAAC ACCESS SOLUTION
FDA Adverse Event
Injury
·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ITI·November 3, 2014