8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
ROOT CANAL FILES, TYPE H (HEDSTROM
FDA 510(k)
FDA Class 1
·Dental
Legacy
FDA UDI
Gc Orthodontics America Inc.·E53582262200001·LEGACY 1. MOLAR UPR LFT SZ 22
ENDURAMESH
FDA 510(k)
FDA Class 2
·Orthopedic
CEM-OSTETIC, MODELS CEMO-020O, CEMO-05P, CEMO-10P, CEMO-20P, AND CEMO-30P
FDA 510(k)
FDA Class 2
·Orthopedic
HS HAND CONTROLLED CURVED SHEA
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GEI·November 27, 2007
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·November 7, 2012
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2014
Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018