14 results · 20ms · Sources: EU EUDAMED, US FDA

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AERO DV TRACHEOBRONCHIAL STENT SYSTEM

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

Harvard PremiumFill OptiTips A3

FDA UDI
Harvard Dental International GmbH·EHAR70836251·Universal light cure nano-hybrid composite for ...

NASALGUARD

FDA 510(k)
FDA Class 2 ·General Hospital

PERMACOL

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

STEM: QUADRA-H CEMENTLESS, HA COATED LAT STEM SIZE 2

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·December 3, 2019

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·February 4, 2026

G7 CURVED INSERTER THD SHAFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·September 30, 2025

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·April 29, 2013

QUICKSITE LV

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code OJX·May 10, 2011

ACCU-CHEK COMPACT TEST DRUM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 29, 2008

G7 CURVED INSERTER THD SHAFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·February 21, 2024

G7 CURVED INSERTER THD SHAFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·February 21, 2024

PLATE,FIXATION,BONE

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HRS·May 9, 2014

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