10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LOGIQ E9, LOGIQ E9 XDClear 2.0
FDA 510(k)
FDA Class 2
·Radiology
BIOLAND G-423 GLOOD GLUCOSE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ECG PEN
FDA 510(k)
FDA Class 2
·Cardiovascular
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE5/11 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·July 27, 2018
Widex
FDA UDI
Widex A/S·05706069792874·Widex UNIQUE U-PA (Shocking pink ) 50, RC coil
Widex
FDA UDI
Widex A/S·05706069819571·Widex UNIQUE U-FS (Shocking pink ) 50, Telecoil...
EXTENSION SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 15, 2011
3 CC SAF. SYR 23X1
FDA Adverse Event
Other
·COVIDIEN·Product code FMF·May 29, 2013
ONE TOUCH ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·September 15, 2008
RECLAIM DISTAL TAPERED Distal Stem, various sizes. Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the locking taper surface of the Distal Stem is protected during proximal preparation.
FDA Enforcement
Class II
·Terminated·DePuy Orthopaedics, Inc.·July 30, 2014