13 results
·
19ms
·
Sources: EU EUDAMED, US FDA
PHENCYCLIDINE URINE ASSAY
FDA 510(k)
FDA Unclassified
·Unknown
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77904011·Mini Sprint Bracket McLaugh/Benn/Trev. .022" ma...
Coblation
FDA UDI
Smith & Nephew, Inc.·00817470001419·PERC DC (OLD)
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77904010101·Mini Sprint Bracket McLaugh/Benn/Trev. .022" ma...
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77904010051·Mini Sprint Bracket McLaugh/Benn/Trev. .022" ma...
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77904011001·Mini Sprint Bracket McLaugh/Benn/Trev. .022" ma...
ORTHOSS
FDA 510(k)
FDA Class 2
·Orthopedic
MAMBA and MAMBA Flex Microcatheters
FDA 510(k)
FDA Class 2
·Cardiovascular
MAMBA? FLEX
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQY·September 11, 2025
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·June 4, 2019
12/14 ARTICUL 44MM M SPEC+15.5
FDA Adverse Event
Injury
·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code LPH·May 5, 2014
EXTERNAL PULSE GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 2, 2007