14 results · 25ms · Sources: EU EUDAMED, US FDA

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RADIONUCLIDE BRACHYTHERAPY SOURCE

FDA 510(k)
FDA Class 2 ·Radiology

RTE SNAPCONE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FHW·July 11, 2023

SPACELABS MEDICAL ANESTHESIA DELIVERY SYSTEM (ADS) WITH PRESSURE CONTROL MODE

FDA 510(k)
FDA Class 2 ·Anesthesiology

CEMENT RESTRICTOR

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

REAR TIP EXTENDER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code N/A·December 30, 2025

RTE SNAPCONE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FHW·February 17, 2021

COLONRING/COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI MEDICAL TECHNOLOGIES LTD.·Product code FZP·September 2, 2011

COLONRING/COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 26, 2011

ENDO SMARTCAP

FDA Adverse Event
MEDIVATORS·Product code KOG·February 2, 2015

NEXGEN PROLONG LPS-FLEX ARTICULAR SURFACE

FDA Adverse Event
Injury ·ZIMMER INC·Product code JWH·May 1, 2013

UNKNOWN DEPUY LCS PATELLA

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HTG·May 12, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 5, 2008

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

Fortify Assura, Sterile EO, Model #/ Part #: CD1257-40/100042322, 100059623; CD1257-40Q/100042341, 100059535; CD1259-40/100041914, 100042338, 100059536, 100059646, 100081567; CD1259-40Q/100041931, 100042339, 100059537, 100059620, 100059626, 100078685; CD1263-40/100042948; CD1263-40Q/100042949; CD1357-40C/100080365, 100080377, 100083441; CD1357-40Q/100080389, 100080390, 100083388; CD1359-40/100078740, 100083267, 100096839; CD1359-40C/100078500, 100078969, 100079372, 100079373, 100083442, 100083443, 100117545; CD1359-40Q/100078804, 100079155, 100079413, 100083445, 100096884; CD1359-40QC/100078603, 100079145, 100079146, 100079239, 100083405, 100083444, 100117632, 100127000, 100127065; CD1363-40C/100080349; CD1363-40Q/100080317; CD1391-40C/100080756; CD1391-40QC/100080783; CD2257-40/100042337, 100059839; CD2257-40Q/100042342, 100059842; CD2259-40/100041893, 100042308, 100059794, 100059907, 100082567; CD2259-40Q/100041894, 100042309, 100059845, 100059873, 100078610; CD2263-40/100042950; CD2263-40Q/100043201; CD2357-40C/100080404, 100080413, 100083490; CD2357-40Q/100080319, 100080412, 100083492; CD2359-40/100078750, 100083466; CD2359-40C/100078651, 100079201, 100079240, 100079442, 100083501, 100083502, 100117546; CD2359-40Q/100078841, 100079109, 100083472; CD2359-40QC/100078652, 100079156, 100079157, 100079337, 100083407, 100083465, 100117580, 100127092, 100127103; CD2363-40C/100080416; CD2363-40Q/100080407; CD2391-40C/100080784; CD2391-40QC/100080744

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