16 results · 22ms · Sources: EU EUDAMED, US FDA

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NeoMatriX Wound Matrix

FDA 510(k)
FDA Unclassified ·Unknown

Lateral Patient Positioning System

FDA UDI
ALPHATEC SPINE, INC.·00190376484198·Pelvic Posterior Paddle

CAREVENT PAR (PUBLIC ACCESS RESUSCITATOR)

FDA 510(k)
FDA Class 2 ·Anesthesiology

MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS, MIDWEST REPROCESSING CENTER REPROCESSED ALP SLE

FDA 510(k)
FDA Class 2 ·Cardiovascular

FLOGARD

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 17, 2014

TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·June 21, 2013

GENESIS 8-CHANNEL RECHARGEABLE IPG

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 21, 2011

LACTO SCR 2.0X7MM 2.0 SYS 2/PK

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code JEY·December 15, 2021

L-PLT LT REG 2.0 LACTOSORB SYS

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code HRS·December 15, 2021

LACTO SCR 2.0X7MM 2.0 SYS 2/PK

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code JEY·December 15, 2021

LACTO SCR 2.0X7MM 2.0 SYS 2/PK

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code JEY·December 15, 2021

LACTO SCR 2.0X7MM 2.0 SYS 2/PK

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code JEY·December 16, 2021

LACTO SCR 2.0X7MM 2.0 SYS 2/PK

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code JEY·December 15, 2021

LACTO SCR 2.0X7MM 2.0 SYS 2/PK

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code JEY·December 15, 2021

LACTO SCR 2.0X7MM 2.0 SYS 2/PK

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code JEY·December 15, 2021

LACTO SCR 2.0X7MM 2.0 SYS 2/PK

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code JEY·December 15, 2021