10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
SAPHIRE PLUS SURGICAL MIRROR
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
DISPOSABLE FIBER OPTIC DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PHONAK PICO-FORTE PP-SC-2 BTE HEARING INSTRUMENT
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FET·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FET·May 23, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FET·February 4, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FET·September 14, 2021
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·December 21, 2010
HT70 VENTILATOR
FDA Adverse Event
Malfunction
·NEWPORT MEDICAL INSTRUMENTS·Product code CBK·January 4, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·February 4, 2014