24 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CorPath GRX System
FDA 510(k)
FDA Class 2
·Cardiovascular
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112601·BARRON CORNEAL PUNCH 7.25MM
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113523·SLIT BLADE 3.0MM STR (BX/5)
Trifocus
FDA UDI
Diversified Products, Inc.·00037741220275·
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122308·KWire .078 x 9"(2.0x225mm))
DELTA 32; DELTA 32 TACT
FDA 510(k)
FDA Class 2
·Radiology
THERMEDX 37-5 ELECTROCAUTERY PROBES, MODELS MPJ200, MPJ210, MPS220, MPN230, BPH240
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DERMABOND PRINEO
FDA Adverse Event
Injury
·ETHICON - 3M / ETHICON, INC.·Product code OMD·October 21, 2022
TENDRIL SDX
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CARDIAC RHYTHM MANAGEMENT DIVISI·Product code NVN·January 13, 2014
PATROL PUMP
FDA Adverse Event
Malfunction
·ABBOTT NUTRITION·Product code LZH·August 5, 2011
MP70 INTELLIVUE PATIENT MONITOR
FDA Adverse Event
Death
·PHILIPS MEDICAL SYSTEMS·Product code DSI·June 24, 2013
UNKNOWN AVENIR STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022
UNKNOWN AVENIR STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·June 8, 2022
UNKNOWN AVENIR STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022
UNKNOWN AVENIR STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022
UNKNOWN AVENIR STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·June 8, 2022
UNKNOWN AVENIR STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022
UNKNOWN AVENIR STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·June 8, 2022
UNKNOWN AVENIR STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022
UNKNOWN BROACH
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·June 8, 2022