16 results · 29ms · Sources: EU EUDAMED, US FDA

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OHMEDA MEDICAL GIRAFFE OMNIBED

FDA 510(k)
FDA Class 2 ·General Hospital

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704292893·

NA

FDA UDI
KEY SURGICAL, INC.·10849771049217·K-Wires, Single trocar, .062-inch (1.6mm) diame...

mahe medical GmbH

FDA UDI
mahe medical gmbh·04050659484436·K-Wire w. trocar/round end _x000D_...

K-Wire w. trocar/round end 1.57mm/127mm, 6 pcs./unit

FDA UDI
mahe medical gmbh·EMAHKM711750·K-Wire w. trocar/round end 1.57mm...

CONMED

FDA UDI
Conmed Corporation·10845854008973·OSCILLATOR ABRADER BLADE, 20 X 46 MM

W.O.M. LASER U100

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

SERAGARD VASCULAR ACCESS PATCH

FDA 510(k)
FDA Class 2 ·General Hospital

SPECTRA WAVEWRITER?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·February 2, 2026

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·March 26, 2025

COAGUCHEK ® XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·April 22, 2013

ECHELON

FDA Adverse Event
Injury ·SMITH & NEPHEW, ORTHOPEDICS·Product code JDH·April 27, 2011

GE OEC 9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEM INC.·Product code JAA·July 10, 2008

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Injury ·SYNTHES USA·Product code KWP·May 13, 2016

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Injury ·SYNTHES USA·Product code KWP·May 13, 2016

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