4,997 results · 33ms · Sources: EU EUDAMED, US FDA

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Force Fiber Fusion Suture

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

Surgineedle

FDA UDI
Covidien LP·20884521080819·Insufflation Needle

OsteoMed

FDA UDI
OSTEOMED LLC·00845694027014·2.0mm X 16mm Cannulated Headless Screw

External Fixation

FDA UDI
Life Spine, Inc.·00190837022976·16mm Bolt

HORICO

FDA UDI
Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1720165·Rotary diamond instrument

HORICO

FDA UDI
Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1720162·Rotary diamond instrument

FG Dental Burs

FDA UDI
BIOLINE DENTAL IMPLANT SYSTEMS LTD·07290119311651·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694068468·Cannulated 2.0 x 16mm Headless Screw Sterile Qty 5

CUP ELECTRODES, GOLD, REUSABLE, SILVER, REUSABLE; CUP ELECTRODES SILVER/SILVER CHLORIDE REUSABLE

FDA 510(k)
FDA Class 2 ·Neurology

PRECICONTROL CLINCHEM MULTI 1 AND 2

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

BARD TEGRESS URETHRAL BULKING AGENT

FDA Adverse Event
Injury ·C.R. BARD, INC.·Product code LNM·March 28, 2007

CARTO RMT SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER, LTD (HAIFA, ISRAEL)·Product code DQK·September 19, 2008

BIA400 IMPLANT 4MM W ABUTMENT 10MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·November 16, 2016

NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR LTD.·Product code MCM·February 16, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·August 30, 2016

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·October 16, 2016

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 1, 2016

CONAIR

FDA Adverse Event
Injury ·CONAIR CORPORATION·Product code MNW·October 17, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·December 15, 2016