8 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INUMI Flex Needle
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RANDOX AMIKACIN
FDA 510(k)
FDA Class 2
·Clinical Toxicology
BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM
FDA 510(k)
FDA Class 2
·Dental
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 22, 2025
BD¿ SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·May 18, 2018
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·September 4, 2011
NAVISTAR RMT THERMOCOOL DIAGNOSTIC/ABLATION STREERABLE TIP CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code OAD·November 13, 2008
GYNECARE TVT RETROPUBIC SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·July 18, 2013