10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
GRAVITYTM PEEK-OPTIMA Suture Anchor
FDA 510(k)
FDA Class 2
·Orthopedic
Well at Walgreens
FDA UDI
WALGREEN CO.·00049022632837·Plastic Applicator Tampon, Super absorbency 36
DIAMOND ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DIAGNOSTIC HYBRIDS' D3 DFA HERPES SIMPLEX VIRUS IDENTIFICATION AND TYPING KIT, MODEL 01-090000
FDA 510(k)
FDA Class 2
·Microbiology
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 24, 2021
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 1, 2022
N/A
FDA Adverse Event
Malfunction
·NEURO - VILLALBA·Product code LGW·June 14, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·July 20, 2011
LACTOSORB PECTUS STABILIZER
FDA Adverse Event
Malfunction
·BIOMED MICFORFIXATION·Product code HRS·September 10, 2008
GRASS PLATINUM SUBDERMAL NEEDLE ELECTRODE
FDA Adverse Event
Malfunction
·NATUS MANUFACTURING LTD·Product code GXZ·December 16, 2019