16 results · 28ms · Sources: EU EUDAMED, US FDA

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SILASTIC BRAND FOLEY CATHETER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Lumbar Catheter

FDA UDI
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)·10381780034247·The Integra Y- Lumbar Catheter consists of a F5...

Steri Irrigation Tip

FDA UDI
DiaDent Group International·08806383562454·Steri Irrigation Tip Side Open Type designed as...

HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY

FDA 510(k)
FDA Class 2 ·Ophthalmic

ASAHI Corsair Microcatheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

ASR UNI FEMORAL IMPL SIZE 49

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·February 8, 2013

BIOMET

FDA Adverse Event
Injury ·Product code KWA·December 29, 2010

V200 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·July 22, 2014

AIA-900

FDA Adverse Event
Injury ·TOSOH CORPORATION·Product code KHO·February 24, 2016

8100 ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·January 10, 2021

ACIST

FDA Adverse Event
Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007

TOSOH AIA-900

FDA Adverse Event
Injury ·TOSOH CORPORATION·Product code KHO·December 13, 2016

A1A-600II

FDA Adverse Event
Injury ·TOSOH CORPORATION·Product code KHO·October 28, 2016

TOSOH AIA-1800

FDA Adverse Event
Injury ·TOSOH CORPORATION·Product code KHO·November 11, 2016

AIA-360

FDA Adverse Event
Injury ·TOSOH CORPORATION·Product code KHO·March 3, 2016

Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·April 10, 2024