747 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TAPER SET HIP SYSTEM RDP STEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813834·GENUMEDI PRO SILVER SIZE III
ArgenZ Anterior 95x14 #3
FDA UDI
ARGEN CORPORATION, THE·D818121263·Dental porcelain/ceramic restoration kit
CRYO.S
FDA UDI
Greiner Bio - One GmbH·14039943000023·
CORNEAL TREPHINE BLADE
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896072466·CORNEAL TREPHINE BLADE
CRYO.S
FDA UDI
Greiner Bio - One GmbH·14039943001686·
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383505840·Gutta Percha Points is used to root canal filin...
MODIFICATION TO SPARC SLING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LIMA-LTO SMR SHOULDER SYSTEM - FINNED HUMERAL STEMS, LIMA-LTO SMR SHOULDER SYSTEM - FINNED HUMERAL BODIES,
FDA 510(k)
FDA Class 2
·Orthopedic
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 12, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024
BIPAP A40
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 9, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 6, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 13, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 13, 2011
45MM ARTICNG LNR CUTR/6 ROW BL
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code GDW·August 18, 2008
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 16, 2024
BIPAP A40 PRO, IT
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 5, 2025
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 5, 2024