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

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OMNILUX CLEAR-U

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

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810057370953·GETTINGE / SHAMPANE 1400 1500 1900 SOFTCARE PLU...

Specials

FDA UDI
Seaspine Orthopedics Corporation·10889981291204·Trial Rasp, 14 x 13 x 7mm, 7° Lordosis

FERRIS POLYMEM SILVER WOUND DRESSING

FDA 510(k)
FDA Unclassified ·Unknown

CONTINUUM KNEE SYSTEM-PS FEMORAL COMPONENTS- POROUS, MODEL XX-YYY-ZZZZZ

FDA 510(k)
FDA Class 2 ·Orthopedic

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Injury ·CONCENTRIC MEDICAL·Product code NRY·December 14, 2012

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·April 26, 2013

RESTORE ULTRA

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·April 21, 2011

WINGSPAN STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC, NEUROVASCULAR DIV.·Product code NJE·July 22, 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