16 results · 29ms · Sources: EU EUDAMED, US FDA

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MED SCULPT

FDA 510(k)
FDA Class 2 ·Physical Medicine

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00530411·

JOBST forMen

FDA UDI
BSN MEDICAL, INC.·04042809845181·FOR MEN 20-30 MM HG KNEE HIGH CLOSED TOE MEDIUM...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450333747·

PLEXOLONG SETS

FDA 510(k)
FDA Class 2 ·Anesthesiology

ULTRASOUND SCANNER TYPE 2101

FDA 510(k)
FDA Class 2 ·Radiology

ABBOTT PERCLOSE PROGLIDE 6FR

FDA Adverse Event
ABBOTT VASCULAR·Product code MGB·November 24, 2021

PERCLOSE¿ PROSTYLE¿

FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·October 31, 2024

PERCLOSE¿ PROSTYLE¿

FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code MGB·February 10, 2025

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code MGB·January 24, 2022

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code MGB·January 21, 2022

SOFTCLIX ® LANCET DEVICE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·April 11, 2013

SPRINT QUATTRO SECURE

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 13, 2011

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC·Product code LFR·May 30, 2008

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·August 23, 2017

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