7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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POLYMER-COATED, POWDER-FREE, LATEX PATIENT EXAMINATION GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
MODIFICATION TO ZENIEVA
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
FEMALE CONTINENCE DEVICE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 28, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·February 10, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code KWP·August 6, 2014
BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HWC·June 3, 2016