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

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Accure Laser System

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

MAS PLIF

FDA UDI
Nuvasive, Inc.·00887517444714·MAS PLIF Fixation Rod, 35mm Pre-Bent

MITEK

FDA UDI
Medos International Sàrl·10886705029099·Sheath with 1 Rotating Stopcock compatible with...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613017972·K-Wire, Single Ended, Trocar Point, Diameter Si...

n/a

FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM59002421060351·Rotary instrument for ENT surgery

NA

FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295122630·REV INST STER TRAY LOWER

GLUCOCARD 01-MINI BLOOD GLUCOSE MONITORING SYSTEM, RELION MICRO BLOOD GLUCOSE MONITORING SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

ALUMINA HEAD

FDA 510(k)
FDA Class 2 ·Orthopedic

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 29, 2025

GYNECARE X-TRACT MORCELLATOR

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code HET·September 9, 2011

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures. Distributed individually and in kits.

FDA Enforcement
Class II ·Terminated·Applied Medical Resources Corp·May 18, 2016