10 results · 23ms · Sources: EU EUDAMED, US FDA

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GenPrime Snap-Top Split Key Cup

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

ForPro

FDA UDI
Tng Worldwide, Inc.·00672047101387·Blue Nitrile Glove Size Medium 100ct

Biogel

FDA UDI
Bosma Enterprises·10818634023824·Biogel Skinsense Indicator Underglove Surgical ...

SOMATOM SENSATION 64 AND SENSATION CARDIAC

FDA 510(k)
FDA Class 2 ·Radiology

MARROMAX B ONE MARROW ASPIRATION NEEDLE KIT, MODELS 50083-XX, 50084-XX

FDA 510(k)
FDA Class 2 ·General Hospital

ASR ACETABULAR CUPS 50

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·May 31, 2013

GOBED II

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·June 15, 2011

STERRAD 200 STERILIZATION SYSTEM SINGLE-DOOR UNIT WITH STAINLESS STEEL EXTERIOR

FDA Adverse Event
Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·August 28, 2008

Retractor f/Sciatic Nerve Long; Part number: 03.100.014; UDI: 10886982070630

FDA Enforcement
Class II ·Terminated·Synthes (USA) Products LLC·May 16, 2018

PKG, MARYLAND FORCEPS, CURVED LEFT, P/N 0250080282. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.

FDA Enforcement
Class II ·Terminated·Stryker Endoscopy·December 24, 2014