34 results · 20ms · Sources: EU EUDAMED, US FDA

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Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/Divider

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Oticon

FDA UDI
Oticon A/S·05707131334565·OPN 2, KIT 312 2.4G NFM 90 PB R C001

ACHIEVE MAPPING CATHETER AND ELECTRICAL CABLE

FDA 510(k)
FDA Class 2 ·Cardiovascular

GAMMALOC SYSTEM, MODEL 03-00001

FDA 510(k)
FDA Class 1 ·Radiology

PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 31, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 30, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 20, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 8, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 20, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 23, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 29, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 24, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 27, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 22, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 16, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

HARMONIC SCALPEL GENERATOR

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·October 3, 2008