17 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SILKRO
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Brisbane ALIF Cage
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215018436·
Advantage ALIF Trial Cage
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215067977·
EZTETIC DENTAL IMPLANT, 3.1MM DIAMETER, 2.9MMD PLATFORM, 11.5MM LENGTH
FDA Adverse Event
Malfunction
·ZIMMER DENTAL·Product code DZE·April 22, 2021
BD LOGIC BLOOD GLUCOSE MONITOR
FDA Adverse Event
Other
·BECTON DICKINSON·Product code NBW·November 4, 2005
STRATUSOCT WITH RNFL & MACULA NORMATIVE DATABASE
FDA 510(k)
FDA Class 2
·Ophthalmic
NON STERILE, POWEDER FREE BLUE NITRILE EXAMINATION GLOVES - 8623F
FDA 510(k)
FDA Class 1
·General Hospital
MECTALIF ANT - LAG
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code OVD·April 12, 2024
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147526·PS Tibia Insert Trial Size A, 23mm - Right
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523145386·R UHMWPE PS Tibial Insert Sz A 23mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144075·R CIMA HXL PS Tibial Insert Sz A 23mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172672·PS Tibia Insert Trial with Posterior Pin Relief...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143306·R E-CIMA Vitamin E PS Tibial Insert Sz A 23mm
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 18, 2008
MAESTRO HANDSWITCH DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code HBB·July 22, 2011
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·July 18, 2013
Model Number L111, ESSENTIO DR SL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025