9 results · 19ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

FISHER-PICKERING INTRAOCULAR EYE MAGNET

FDA 510(k)
FDA Class 1 ·Ophthalmic

BD¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·May 21, 2018

STACKHOUSE LENS HOOD, MODEL SA-700/FS

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

VIRTUOSAPH (TM) ENDOSCOPIC VEIN HARVESTING DISPOSABLE SYSTEM, MODEL MCVS550

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 9, 2014

PROGRASP (TM) FORCEPS

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·October 24, 2012

FREESTYLE

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·September 10, 2007

BD¿ SYRINGE S2

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 12, 2018

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