86 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACUTRON
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EASYPOINT NEEDLE
FDA Adverse Event
Injury
·RETRACTABLE TECHNOLOGIES, INC.·Product code FMI·February 9, 2023
EASYPOINT NEEDLE
FDA Adverse Event
Injury
·RETRACTABLE TECHNOLOGIES, INC.·Product code FMI·February 9, 2023
TALOS®-C HA
FDA UDI
MEDITECH SPINE, LLC·B167522110000·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16721312110000·
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702401073·Elvarex 2/Thigh High/Slant-Open Toe/Dotted Sili...
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001322110000·Retention Plate, Oblique-Only, Medium, 10 mm
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001332110000·Retention Plate, Oblique-Only, Large, 10 mm
TRAM 2001 MODULE
FDA 510(k)
FDA Class 2
·Cardiovascular
PARCUS 2.0MM / 2.5MM / 3.5MM MITI TITANIUM SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
Immunalysis
FDA UDI
IMMUNALYSIS CORP·00840937105283·Oxycodone Antibody Analyte Specific Reagent (ASR)
Materialise Personalized Solutions
FDA UDI
Materialise NV·05420060343063·Clavicle Osteotomy Guide
GMK TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 22, 2025
LUMAX 540 DR-T
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code MRM·October 29, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·July 8, 2013
DEXTRUS 4136
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVN·November 9, 2015
GMK TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2026
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·November 7, 2024
GMK PRIMARY TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·March 21, 2025
GMK TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·March 3, 2026