10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NATURAL BRIDGE LP TRANSVERSE CONNECTORS
FDA 510(k)
FDA Class 2
·Orthopedic
ShurFit Interbody Device
FDA UDI
PRECISION SPINE, INC.·00840019910040·TPLIF Cage Peek 14mm x 29mm
ShurFit 2C Lumbar Interbody
FDA UDI
PRECISION SPINE, INC.·00840019929899·14mm x 29mm 2C TPLIF Cage PEEK
RHYTHMLINK INTERNATIONAL SUBDERMAL NEEDLE ELECTRODES
FDA 510(k)
FDA Class 2
·Neurology
SONICWAVE SONIC PLAQUE REMOVER
FDA 510(k)
FDA Class 1
·Dental
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 27, 2025
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·April 23, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·April 2, 2011
*
FDA Adverse Event
Injury
·MEDTRONIC MILACA INC.·Product code DTE·July 10, 2008
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