11 results · 28ms · Sources: EU EUDAMED, US FDA

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LOOP RECORDER VITAPHONE, 3100 SERIES

FDA 510(k)
FDA Class 2 ·Cardiovascular

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496053378·NIGHT WELLNESS 70, SIZE L, ROSA, GRADUATED COMP...

EBI XFIX DFS SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ORIA CLARIS

FDA 510(k)
FDA Class 2 ·Orthopedic

EQUINOXE REVERSE SHOULDER COMPONENTS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code HSD·August 20, 2024

OPTIFLEX?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFL·April 11, 2013

OT VERIO IQ METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 3, 2014

SPRINT FIDELIS

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

Exactech Acapella One Interbody Fusion Device Parallel. Orthopedic Spinal Surgery Device. Product Usage: The Acapella One Cervical Spacer System is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with degenerative disc disease at one disc level from C2-T1. Is to be used with autogenous bone graft and supplemental internal fixation and is implanted via an open anterior approach.

FDA Enforcement
Class II ·Terminated·Exactech, Inc.·February 24, 2016

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

Unify Assura, Sterile EO, Model #/ Part #: CD3257-40/100042333, 100059944; CD3257-40Q/100042334, 100059936; CD3261-40/100048460, 100048546, 100059897, 100059954, 100059996, 100078828; CD3261-40Q/100048568, 100048581, 100059898, 100059955, 100059997, 100078853; CD3357-40C/100080408, 100080424, 100083511; CD3357-40Q/100080419, 100080463, 100083504; CD3361-40/100078842, 100079211, 100083506, 100096893; CD3361-40C/100078604, 100079159, 100079160, 100079338, 100083429, 100083514, 100117625; CD3361-40Q/100078805, 100079222, 100079456, 100083523, 100098067; CD3361-40QC/100078654, 100079202, 100079221, 100083475, 100083515, 100117558; CD3389-40C/100080778; CD3389-40QC/100080780, 100105489

FDA Enforcement
Class II ·Terminated·St Jude Medical Inc.·July 4, 2018