15 results · 19ms · Sources: EU EUDAMED, US FDA

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HANN-VAC TM, DISPOSABLE,SUCTION CATHETER

FDA 510(k)
FDA Class 1 ·Anesthesiology

Brigade

FDA UDI
Nuvasive, Inc.·00887517962928·Brigade Lateral Trial, 14x34x32mm 25°

BIOFIND

FDA 510(k)
FDA Class 2 ·Neurology

CUATTRO UNOMD

FDA 510(k)
FDA Class 2 ·Radiology

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 5, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 5, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 5, 2024

ARCOMXL POLYETHYLENE LINER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LZO·August 31, 2017

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·June 30, 2014

UNKNOWN WOMEN'S HEALTH PRODUCT

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON)·Product code FTL·January 3, 2013

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 26, 2007

STEALTHSTATION¿ S8 SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·January 21, 2026

Titanium Tack Starter Kit, REF 400-270, Rx Only, non-sterile, BIOHORIZONS, BIRMINGHAM, AL 35244. Dental.

FDA Enforcement
Class II ·Terminated·BioHorizons Implant Systems Inc·December 26, 2012

STEALTHSTATION S8 SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·October 8, 2021

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