7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
URESIL CLOSED DRAINAGE RESERVOIR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ARIETTA PRECISION
FDA 510(k)
FDA Class 2
·Radiology
VISUALASE ENVISION SOFTWARE SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
CONSULTA CRT-P
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NVZ·June 10, 2014
VIRTUOSO DR
FDA Adverse Event
Death
·MEDTRONIC MED REL, INC.·Product code LWS·October 11, 2010
TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code LOX·December 10, 2012
Zeiss brand IOLMaster, Version 1-5, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactured by Carl Zeiss Meditec AG (Jena), Carl Zeiss Promenade 10, Jena, Germany 07745; and distributed by Carl Zeiss Meditec, Inc., Dublin, CA This device is intended for use primarily by physicians and health care workers and may be only used under the supervision of a physician. This device will not be sold to the general public. The IOLMaster is intended for the biometric determination of ocular measurements of axial length, anterior chamber depth, corneal radius, white-to white (WTW), and for the measurement of pupil size and deviation of the visual axis from the center of the pupil. For patients who are candidates for intraocular lens (IOL) implantation, the device also performs calculations to assist physicians in determining the appropriate IOL power and type for implantation
FDA Enforcement
Class II
·Terminated·Carl Zeiss Meditec, Inc.·November 27, 2013