7 results · 27ms · Sources: EU EUDAMED, US FDA

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MICRO CULTURE MEDIA P3528, P3137, P3149, P3139

FDA 510(k)
FDA Class 1 ·Microbiology

Legend Acetabular Liners

FDA 510(k)
FDA Class 2 ·Orthopedic

E 310 ELECTROCARDIOGRAPH

FDA 510(k)
FDA Class 2 ·Cardiovascular

FLEXTEND

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVN·October 19, 2010

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 21, 2014

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·December 14, 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