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

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NORIAN SRS BONE VOID FILLER

FDA 510(k)
FDA Class 2 ·Orthopedic

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341933·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341834·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341858·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341902·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341896·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341841·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341919·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341872·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341889·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341865·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033341926·

MULTI-STIM, MODEL MS-100

FDA 510(k)
FDA Class 2 ·Neurology

MERIDIAN-PORTABLE

FDA 510(k)
FDA Class 2 ·Neurology

QUICK SET

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·October 27, 2025

11MM/130 DEG TI CANN TROCH FIXATION NAIL 360MM/LEFT

FDA Adverse Event
Injury ·SYNTHES MONUMENT·Product code HSB·February 11, 2016

2520274-2013-01595

FDA Adverse Event
Malfunction ·SYNTHES (USA) WEST CHESTER, PA·Product code MCV·March 19, 2013

ACCU-CHEK SPIRIT CARTRIDGE

FDA Adverse Event
Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·February 9, 2011

ZENITH AAA ILIAC LEG GRAFT

FDA Adverse Event
Injury ·COOK, 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