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

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Latex Powder Free Polymer Coated Examination Glove with Protein Labeling Claim of 50 Microgram or Less Per Gram of Glove

FDA 510(k)
FDA Class 1 ·General Hospital

OSS™ Orthopedic Salvage System

FDA UDI
Biomet Orthopedics, LLC·00880304250710·

HAMILTON-T1

FDA UDI
Hamilton Medical AG·07630002801850·

OsteoMed

FDA UDI
OSTEOMED LLC·00842528123188·Logic Jr Distractor, 30mm Right

Vilex Power Accessory

FDA UDI
VILEX IN TENNESSEE, INC.·00841731122254·KWire .062x4" (1.6x100mm)

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167311610060·

InSpan®

FDA UDI
SPINEFRONTIER, INC.·00190361000440·InSpan Slim, SP Plate, 12x39mm

InSpan®

FDA UDI
SPINEFRONTIER, INC.·00190361000433·InSpan Slim, SP Plate, 10x37mm

InSpan®

FDA UDI
SPINEFRONTIER, INC.·00190361000464·InSpan Slim, SP Plate, 16x43mm

InSpan®

FDA UDI
SPINEFRONTIER, INC.·00190361000419·InSpan Slim, SP Plate, 8x35mm

InSpan®

FDA UDI
SPINEFRONTIER, INC.·00190361000457·InSpan Slim, SP Plate, 14x41mm

InSpan®

FDA UDI
SPINEFRONTIER, INC.·00190361000426·InSpan Slim, SP Plate, 8x43mm

TALOS® HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321610060·

WAVELIGHT FS200 LASER SYSTEM MODEL: FS200

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

IKOENGELO

FDA 510(k)
FDA Class 2 ·Radiology

PRODIGY AUTOCODE

FDA Adverse Event
Malfunction ·OK BIOTECH CO., LTD.·Product code NBW·December 19, 2017

VEGA SPAN SPINOUS PROCESS PLATE SYSTEM

FDA Adverse Event
Injury ·SPINEFRONTIER INC.·Product code KWP·October 9, 2017

BELLAFILL DERMAL FILLER

FDA Adverse Event
Injury ·SUNEVA MEDICAL, INC.·Product code LMH·February 9, 2018

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013