15 results · 27ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

PROVENT NASAL CANNULA

FDA 510(k)
FDA Class 2 ·Anesthesiology

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014608723·MAQUET 2.25" DELUXE GEL

PLLA PIN

FDA 510(k)
FDA Class 2 ·Orthopedic

CERAMIX PORCELAIN SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

BD INSYTE AUTOGUARD PNK 20GA X 1.16IN

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 19, 2022

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

ICL (IMPLANTABLE COLLAMER LENS)

FDA Adverse Event
Injury ·STAAR SURGICAL COMPANY·Product code MTA·April 26, 2013

840 VENTILATOR

FDA Adverse Event
Malfunction ·PURITAN BENNETT CORP.·Product code CBK·April 13, 2011

FMP ACETABULAR LINERS

FDA Adverse Event
Other ·ENCORE MEDICAL, L.P.·Product code KWB·July 23, 2008

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 12, 2009

1000317571-2021-00127

FDA Adverse Event
Injury ·CONVATEC LTD·Product code FRO·March 17, 2021

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·October 31, 2008

Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

FDA Enforcement
Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015