10 results
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26ms
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Sources: EU EUDAMED, US FDA
RETAINER, SCREW EXPANSION ORTHODONTIC
FDA 510(k)
FDA Class 1
·Dental
Brigade
FDA UDI
Nuvasive, Inc.·00887517963093·Brigade Lateral Trial, 14x38x28mm 8°
FRESENIUS OPTIFLUX 200A
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913
FDA 510(k)
FDA Class 1
·Clinical Chemistry
STEM: MINIMAX CEMENTLESS ANATOMICAL STEM LEFT SIZE 5
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·December 9, 2020
SET SCREW, TI GAMMA3® Ø8X17.5MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code HSB·July 22, 2014
ESSURE
FDA Adverse Event
Injury
·BAYER·Product code HHS·July 9, 2015
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 9, 2013
SIMON NITINOL FILTER SYSTEM
FDA Adverse Event
Injury
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·November 16, 2010
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