17 results · 21ms · Sources: EU EUDAMED, US FDA

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NightOwl

FDA 510(k)
FDA Class 2 ·Anesthesiology

LEONE SPA

FDA UDI
LEONE SPA·08033707022220·CALIBRA BANDS 2ND MOLAR n.SUR 28

Surgical Connector Kit

FDA UDI
Synapse Biomedical, Inc.·00852184003410·

AQUAMAX (ETAFILCON A) DISPOSABLE SOFT CONTACT LENSES

FDA 510(k)
FDA Class 2 ·Ophthalmic

6F MACH1/34356-XXX; 5F MACH1/35845-XXX; 7F MACH1/34357-XXX; 8F MACH1/34358-XXX

FDA 510(k)
FDA Class 2 ·Cardiovascular

RELAY THORACIC STENT-GRAFT WITH PLUS DELIVERY SYSTEM

FDA Adverse Event
Injury ·BOLTON MEDICAL, INC.·Product code MIH·November 7, 2019

Widex

FDA UDI
Widex A/S·05706069797107·Widex D-CIC (Clay brown ) Dream 220, Left, RC coil

Widex

FDA UDI
Widex A/S·05706069887082·WIDEX MOMENT M-IP (Clay brown ) 220, Right

Widex

FDA UDI
Widex A/S·05706069796681·Widex EVOKE E-CIC (Clay brown ) 220, Left, RC coil

Widex

FDA UDI
Widex A/S·05706069819816·Widex UNIQUE U-IP (Clay brown ) 220, Right

Widex

FDA UDI
Widex A/S·05706069796919·Widex EVOKE E-IP (Clay brown ) 220, Right

Widex

FDA UDI
Widex A/S·05706069888959·WIDEX MOMENT M-CIC (Clay brown ) 220, Left

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 3, 2014

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 12, 2011

QUADRA ASSURA CRT-D, DF4 CONNECTOR

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·July 11, 2013

DAVINCI 5

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 25, 2026

CLS SPOTORNO, STEM, 135, UNCEMENTED, 10.0, TAPER 12/14

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code LZO·March 20, 2018