16 results
·
21ms
·
Sources: EU EUDAMED, US FDA
URINARY DRAIN BAG, LSL CAT. NO. 1425 AND 1450
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
Arthrex®
FDA UDI
ARTHREX, INC.·00888867386525·Cortical Screw, 2.7 mm x 14 mm
Arthrex®
FDA UDI
ARTHREX, INC.·00888867046757·LO-PRO SCRW TM SS 2.7X 14MMCORTEX
Novidia Bulk Fill Flow Composite
FDA 510(k)
FDA Class 2
·Dental
AUDIT MICROCV THERAPEUTIC DRUG (TDM) LINEARITY SET, MODEL K707M-5
FDA 510(k)
FDA Class 1
·Clinical Chemistry
LO-PRO SCRW TM SS 2.7X 14MMCORTEX
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·July 14, 2023
ST FRANCIS HSP TULSA OK 1
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DTZ·December 18, 2012
LO-PRO LOCK SCRW,SS 2.7X 14MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWC·June 6, 2024
SYMBIQ DCHANNEL 3.01
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·April 10, 2014
EON MINI 16-CHANNEL IPG
FDA Adverse Event
Malfunction
·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·October 13, 2010
ENDURANT II ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·December 20, 2012
LO-PRO SCRW TM,SS 3.5X 14MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·July 14, 2023
LO-PRO SCRW TM,SS 3.5X 18MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·July 14, 2023
CLAV FRAC PLT,CENTRAL THIRD,LFT,SS
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 15, 2023
LO-PRO LOCK SCRW,SS 3.5X 14MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 4, 2023
LO-PRO SCRW TM,SS 3.5X 16MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·July 14, 2023