14 results · 23ms · Sources: EU EUDAMED, US FDA

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INSULIN PUMP

FDA 510(k)
FDA Class 2 ·General Hospital

N/A

FDA UDI
GEORGE TIEMANN & CO.·B5821051041·HOOK, SURGICAL, GENERAL & PLASTIC SURGERY

NA

FDA UDI
Stryker GmbH·00886385010397·Drill Bit, Quick Connect

WATERLASE, MILLENNIUM

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

AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED, AGC-GOLDBONDER, AGC GLAVANOGOLD

FDA 510(k)
FDA Class 2 ·Dental

PERCLOSE PROSTYLE SUTURE-MEDIATED CLOSURE AND REPAIR SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code MGB·December 7, 2023

ADAPTA

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·April 10, 2013

MALLINCKRODT

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code BTR·April 4, 2011

IDENTITY ADX SR

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008

PERCLOSE¿ PROSTYLE¿

FDA Adverse Event
Malfunction ·ABBOTT VASCULAR INC.·Product code MGB·November 10, 2025

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·October 1, 2010

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code MGB·November 23, 2020

PERCLOSE PROSTYLE SUTURE-MEDIATED CLOSURE AND REPAIR SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code MGB·February 13, 2024

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012