8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BIOMET RECONSTRUCTIVE WEDGES MODEL 110003660-99, 110003797-831
FDA 510(k)
FDA Class 2
·Orthopedic
ArgenZ HT+ 95x20 OM3
FDA UDI
ARGEN CORPORATION, THE·D818122770·Dental porcelain/ceramic restoration kit
FLEXTIME FAST & SCAN PUTTY, FLEXTIME FAST & SCAN LIGHT FLOW, FLEXTIME FAST & SCAN MEDIUM FLOW
FDA 510(k)
FDA Class 2
·Dental
NVISION VLE IMAGING SYSTEM, NVISION VLE CATHETER
FDA 510(k)
FDA Class 2
·Radiology
PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·September 24, 2018
ENDOPATH** XCEL* BLADELESS TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·May 21, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 18, 2014
ASR ACETABULAR IMPLANT 62
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code KWA·June 3, 2011