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

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Disposable Blade

FDA UDI
KATENA PRODUCTS, INC.·00841668113202·BARD-PARKER BLADE #15 PACK OF 50

KardiaAI

FDA 510(k)
FDA Class 2 ·Cardiovascular

Disposable Blade

FDA UDI
KATENA PRODUCTS, INC.·00841668113196·BARD-PARKER BLADE #11 PACK OF 50

INTRODEUCE DOUBLE LUMEN INTRODUCER

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEDX LCS LASER SERIES

FDA 510(k)
FDA Class 2 ·Physical Medicine

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

PIPELINE

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 24, 2019

INTRAMEDULLARY ARTHRODESIS IMPLANT SMART TOE II 16MM / 0° ANGLE FOR PIP ARTHROD

FDA Adverse Event
Injury ·STRYKER TRAUMA SELZACH·Product code HTY·October 27, 2014

SPRINT QUATTRO SECURE

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011

SM304 M-SERIES W/ZOOM

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code INK·July 2, 2013

UNKNOWN CHLORAPREP

FDA Adverse Event
Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·August 31, 2021

UNK - SCREWS: ZERO-P

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·August 8, 2022

ELUVIATM DRUG-ELUTING VASCULAR STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIU·April 8, 2019

HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

FDA Adverse Event
Death ·HEARTWARE, INC.·Product code DSQ·November 15, 2019

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