21 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Leaf Photocoagulator
FDA 510(k)
FDA Class 2
·Ophthalmic
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690196334·AK3 PS Femoral Trials Size 1 - 5 Right Pan
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306821769·Laryngeal Mirror #3
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101070·WALTON CONJUNCTIVA RETRACTOR
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690195030·AK3 PS Femoral Trials Size 1 - 5 Right Pan Insert
CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090
FDA 510(k)
FDA Class 2
·Dental
ESTHETICA
FDA 510(k)
FDA Class 2
·Dental
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·March 13, 2026
RESPIRONICS
FDA Adverse Event
Malfunction
·Product code MNT·April 8, 2021
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·January 13, 2026
CONFIRM
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code MXC·January 11, 2014
NOVOPEN 3 DEMI
FDA Adverse Event
Other
·NOVO NORDISK A/S·Product code FMF·June 21, 2013
LIGASURE IMPACT THORACIC
FDA Adverse Event
Malfunction
·COVIDIEN LP (VALLEYLAB)·Product code GEI·June 30, 2011
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025