16 results · 27ms · Sources: EU EUDAMED, US FDA

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ANCHORAGE CLOSURE DEVICE

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

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0730060·Rod Bender, 5.5 mm, 5 Position

PHENCYCLIDINE

FDA 510(k)
FDA Unclassified ·Unknown

FASTPACK CALIBRATORS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·March 28, 2024

VIASYS

FDA Adverse Event
Malfunction ·CAREFUSION 207, INC·Product code CBK·October 26, 2009

APPLICATION INSTRUMENT FOR STERNAL ZIPFIX

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code JDQ·April 23, 2013

POWERPORT

FDA Adverse Event
Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code LJT·April 21, 2011

RIATA ACTIVE FIXATION LEAD

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2008

VIASYS

FDA Adverse Event
Other ·CAREFUSION 207, INC·Product code CBK·October 27, 2009

VIASYS

FDA Adverse Event
Other ·CAREFUSION 207, INC.·Product code CBK·October 27, 2009

Product Name: AVEA Ventilator. All Models. The affected devices are cleared under K073069 pm 1/25/2008 and K103211 on 05/06/2011. This device is a Class II medical Device. A continuous ventilator (respirator) is a device intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Adult, pediatric, and neonatal ventilators are included in this generic type of device.

FDA Recall
Terminated ·Carefusion 211 Inc dba Carefusion·Product code CBK·September 5, 2013

Product Name: AVEA¿ Ventilator. All Models. The affected devices are cleared under K073069 pm 1/25/2008 and K103211 on 05/06/2011. This device is a Class II medical Device. A continuous ventilator (respirator) is a device intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Adult, pediatric, and neonatal ventilators are included in this generic type of device.

FDA Enforcement
Class I ·Terminated·Carefusion 211 Inc dba Carefusion·October 9, 2013

Dexcom G4 PLATINUM Receiver Receiver Part Number: MT20649 Receiver (mg/dL), Black; MT20649-PNK, Receiver (mg/dL), Pink; MT20649-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.

FDA Enforcement
Class I ·Terminated·Dexcom Inc·April 20, 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

Exactech Equinoxe CAGE GLENOID, CEMENTED, alpha curvature, Mates with: a) 38, 41, 44 head, Small, Item Number 314-13-02, b) 38, 41, 44 head, Medium, Item Number 314-13-03, c) 38, 41, 44 head, Large, Item Number 314-13-04; Shoulder Arthroplasty

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·April 10, 2024