75 results · 22ms · Sources: EU EUDAMED, US FDA

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TROCHANTERIC REATTACHMENT DEVICE (STANDARD) AND (LONG), MODEL 501-066, 501-067

FDA 510(k)
FDA Class 2 ·Orthopedic

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00170951·

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00170931·

Coulmed

FDA UDI
Coulmed Products Group LLC·10810087352759·Replacement pad for Arthroscopic Stress Post , ...

RANDOX C-REACTIVE PROTEIN

FDA 510(k)
FDA Class 2 ·Immunology

RECUMBENT BATHING SYSTEMS, RHAPSODY AND PRIMO

FDA 510(k)
FDA Class 2 ·Physical Medicine

ECS 25MM STAPLER

FDA Adverse Event
ETHICON·Product code GDW·March 8, 2013

ACCU-CHEK ® AVIVA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 25, 2011

ACCESS 2 IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·February 15, 2008

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 1, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 10, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·June 6, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 5, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·September 14, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·September 14, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·October 7, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·July 7, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 7, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·October 21, 2011

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 22, 2011