22 results
·
36ms
·
Sources: EU EUDAMED, US FDA
PF 5050 PRESSURE UNIT, MODEL PF 5050
FDA 510(k)
FDA Class 2
·Cardiovascular
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343272·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343296·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343241·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343210·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343265·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343302·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343289·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343234·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343258·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033343227·
IMPROVED TRY-IN GEL
FDA 510(k)
FDA Class 2
·Dental
GLOBAL FX POROUS-COATED HUMERAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQY·December 8, 2006
RADIESSE DERMAL FILLER
FDA Adverse Event
Injury
·BIOFORM MEDICAL, INC.·Product code LMH·February 5, 2009
BD INSULIN PEN NEEDLE
FDA Adverse Event
Injury
·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·March 19, 2013
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 9, 2011
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES, INC·Product code MIH·March 11, 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