14 results · 21ms · Sources: EU EUDAMED, US FDA

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AQUACEL Ag Surgical SP Dressing

FDA 510(k)
FDA Unclassified ·Unknown

Head Impactor Bushing

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215080815·

GEMORE MUSCLE CONDITIONER;

FDA 510(k)
FDA Class 2 ·Physical Medicine

AXSOS LOCKING PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE

FDA Adverse Event
Injury ·MPRI·Product code OJX·June 8, 2013

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE·Product code KDJ·July 7, 2011

GE OEC 9900

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

GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 3/11 MM LEFT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 11, 2017

SCREWDRIVER BIT T15, AO FITTING

FDA Adverse Event
Malfunction ·STRYKER GMBH·Product code HWC·October 6, 2017

SCREWDRIVER BIT T15, AO FITTING

FDA Adverse Event
Malfunction ·STRYKER GMBH·Product code HWC·October 6, 2017

BD SHARPS COLL 1.5QT RED

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·March 23, 2022

ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

FDA Enforcement
Class II ·Ongoing·Elekta, Inc.·December 13, 2023

GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. NOVATION CONSTRAINED LINER 28MM ID GROUP 1, REF 134-28-41 b. NOVATION CONSTRAINED LINER 32MM ID GROUP 2, REF 134-32-42 c. NOVATION CONSTRAINED LINER 36MM ID GROUP 3, REF 134-36-43 d. NOVATION CONSTRAINED LINER 36MM ID GROUP 4, REF 134-36-44 e. NOVATION CONSTRAINED LINER 36MM ID GROUP 5, REF 134-36-45

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·September 21, 2022

Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The T2 Arthrodesis Nail is intended for the treatment of Knee Arthrodesis. The design of the T2 Arthrodesis Nail features a unique curvature which incorporates both femur ante curvature and knee valgus bend. Indications: Aseptic failed total knee arthro-plasty with or without bone loss; Failed external fixation, non unions and malunions; Periarticular fractures where repair is not possible; Pathologic fractures and tumor resections; Pseudoarthrosis and correct osteotomy; Ipsilateral femur fractures; and Open and closed femoral fractures.

FDA Enforcement
Class II ·Terminated·Stryker Howmedica Osteonics Corp.·July 25, 2012