8 results · 18ms · Sources: EU EUDAMED, US FDA

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ALLEVYN ISLAND WOUND DRESSING

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

Locator Implant Anchor

FDA UDI
SIC invent AG·ESIC9357051·Locator® Attachment Ø 4.2 mm, GH 0.0 mm, incl. ...

ACID PHOSPHATASE REAGENT SET

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

LAP 3501 HIGH FLOW INSUFFLATOR

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

PEG ALIGNMENT SOUND

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·January 3, 2013

TERUMO CDI 500 BLOOD PARAMETER MONITOR

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 3, 2010

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 15, 2014

VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States Indications for Use: Epilepsy (PMA 970003): The VNS Therapy System is indicated for use as an adjunctive therapy in reducing the frequency of seizures in adults and adolescents over 12 years of age with partial onset seizures that are refractory to antiepileptic medications. Depression (PMA 970003/S050): VNS Therapy is indicated for the adjunctive long-term treatment of chronic or recurrent depression for patients 18 years of age or older who are experiencing a major depressive episode and have not had an adequate response to four or more adequate antidepressant treatments. Indications outside the U.S.: Epilepsy (Non-US): The VNS Therapy System is indicated for use as an adjunctive therapy in reducing the frequency of seizures in patients whose epileptic disorder is dominated by partial seizure (with or without secondary generalization) or generalized seizures that are refractory to antiepileptic medications. AspireSR (Seizure Response) features the Automatic Stimulation Mode which is intended for patients who experience seizures that are associated with cardiac rhythm increases known as ictal tachycardia. Depression (Non-US): The VNS Therapy System is indicated for the treatment of chronic or recurrent depression in patients who are experiencing a treatment-resistant or treatment-intolerant depressive episode.

FDA Enforcement
Class II ·Terminated·Cyberonics, Inc·August 23, 2017