313 results · 24ms · Sources: EU EUDAMED, US FDA

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SYMBIA 6.0

FDA 510(k)
FDA Class 2 ·Radiology

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756614528·Knee Immobilizer

LEONE SPA

FDA UDI
LEONE SPA·08033707010906·CALIBRA 1ST MOL BANDS W/G8025-02 n.UR 6

OsteoMed

FDA UDI
OSTEOMED LLC·00845694026468·MFx Angulated Locking Straight Plate, 4 Hole

CRYOMEGA

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

VITROS CHEMISTRY PRODUCTS DHDL SLIDES, VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 25, VITROS CHEMISTRY PRODUCTS PERFORMACE

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

I-STAT G3+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JJE·August 26, 2010

PEN NDL 32G 4MM 100BX 1200 USA

FDA Adverse Event
Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·February 10, 2025

STELLARTECH COAGULATION CATHETER

FDA Adverse Event
Injury ·STELLARTECH RESEARCH CORP·Product code KNQ·November 3, 2005

CONTOUR CURVED CUTTER STAPLER CS

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GDW·July 14, 2006

LIGAMAX 5

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC (CINCINNATI)·Product code FZP·April 17, 2007

HIRES 90K

FDA Adverse Event
Malfunction ·ADVANCED BIONICS CORP.·Product code MCM·September 5, 2006

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·COCHLEAR LTD.·Product code MCM·December 12, 2006

NEXUS MULTI-DIAMETER CSR AND NXT HELIX SOFT

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code HCG·December 18, 2008

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·June 23, 2006

HIRES 90K

FDA Adverse Event
Malfunction ·ADVANCED BIONICS CORPORATION·Product code MCM·May 9, 2006

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·August 9, 2006

INTERGARD AORTIC ARCH WOVEN VASCULAR PROSTHESIS

FDA Adverse Event
Injury ·INTERVASCULAR·Product code DSY·March 24, 2006

RENU

FDA Adverse Event
Injury ·BAUSCH AND LOMB·Product code LPN·May 17, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEI·July 14, 2006