3,437 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERRAD VELOCITY Biological Indicator/Process Challenge Device and Reader
FDA 510(k)
FDA Class 2
·General Hospital
Bernafon
FDA UDI
Bernafon AG·05711584086995·ZR3, KIT 13 2.4G NFM L BE ZERENA 3
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110973·STERILIZING CASE MEDIUM/SMALL
PIN SCREW
FDA UDI
BK MEDITECH CO.,LTD.·08809155855143·Wire Pin Screw, 2mm Shaft Diameter x 2mm Thread...
COMBAT READY CLAMP
FDA 510(k)
FDA Class 2
·Cardiovascular
FLUID FILLED TEETHER - GEL
FDA 510(k)
FDA Class 2
·Dental
ENDURON 10D 58 OR 70ODX28ID
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HRY·October 6, 2008
AVAULTA SOLO ANTERIOR SYNTHETIC SUPPORT SYSTEM
FDA Adverse Event
Injury
·BARD SHANNON LIMITED·Product code OTP·June 20, 2013
ACHIEVE MAPPING CATHETER
FDA Adverse Event
Injury
·MDT ABLATION FRONTIERS MFG·Product code DRF·August 4, 2011
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·August 21, 2025
MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·November 14, 2025
PUMP 1886 780G OUS BLE PUMP MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·October 8, 2025
BIPOLAR HIGH FREQUENCY CORD, 400 CM
FDA Adverse Event
Injury
·KARL STORZ SE & CO. KG·Product code GEI·March 12, 2025
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·November 11, 2025
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·November 11, 2025
NI
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·May 19, 2025
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·November 11, 2025
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·November 13, 2025
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 17, 2025
MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 18, 2025