634 results · 34ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SYNTHES LOW PROFILE NEURO SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

OsteoMed

FDA UDI
OSTEOMED LLC·00845694008051·2.0mm x 12mm Lag Screw

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193107110·HA PEEK EVOS Straight, ,12mmx9mmx 22mm , BICONV...

OsteoMed

FDA UDI
OSTEOMED LLC·00845694000369·2.0mm x 12mm Screw

OsteoMed

FDA UDI
OSTEOMED LLC·00845694034838·2.0 x 12mm Lag Screw, Sterile

OsteoMed

FDA UDI
OSTEOMED LLC·00845694028769·2.0mm x 12mm Screw, Sterile

OsteoMed

FDA UDI
OSTEOMED LLC·00845694054331·2.0 x 12mm Screw Sterile Qty 10

OsteoMed

FDA UDI
OSTEOMED LLC·00845694066488·HPS 2.0 x 12mm Lag Screw Sterile Qty 5

SYNTHETIC POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

ECG HOME

FDA 510(k)
FDA Class 2 ·Cardiovascular

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·February 29, 2012

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·March 26, 2013

SM304 M-SERIES W/ZOOM

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code INK·March 10, 2011

TUBE, GASTROINTESTINAL (AND ACCESS)

FDA Adverse Event
Injury ·C.R. BARD, INC. (BASD)·Product code KNT·March 31, 2008

ALARIS PCA MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·October 26, 2020

ACRYSOF IQ TORIC

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·July 27, 2012

SKIN PREP 4.25OZ SPR

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code NEC·December 16, 2015

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 27, 2012

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR LTD·Product code MCM·November 2, 2012

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM INC.·Product code MDS·March 28, 2014