9 results
·
27ms
·
Sources: EU EUDAMED, US FDA
AMERICAN SURGICAL SPONGES/NEUROSURGICAL SPONGES
FDA 510(k)
FDA Class 2
·Neurology
P.F.C. SIGMA
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295244585·P.F.C. SIGMA STABILIZED PLUS TIBIAL INSERT TRIA...
TSRH SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TREACE DRILL SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·May 7, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·October 12, 2022
SYMBIQ DCHANNEL 3.01
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·June 13, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 15, 2013
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 13, 2011