36 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VENUS PEARL PLT REFILL A1
FDA 510(k)
FDA Class 2
·Dental
EVOTECH™
FDA UDI
ADVANCED STERILIZATION PRODUCTS SERVICES INC.·10705037048182·Channel Connector Tube, Blue
Biosens cartridges Light Pink
FDA UDI
PERFLEX LTD·07290110501518·box of 6 identical cartridges sealed in a vacuu...
RespiConnect* Adapter
FDA UDI
Trudell Medical International·62860112501020·RespiConnect* Adapter
RespiConnect* Adapter
FDA UDI
Trudell Medical International·00762860125018·RespiConnect* Adapter
ELMED
FDA UDI
ELMED INCORPORATED·00842180163874·Lockhart-Mummery Fistula Probe, Straight
PRINCETON
FDA UDI
Princeton Medical Group, Inc.·00810158214842·PROBE LOCKHART-MUMMERY FISTULA STRAIGHT 6.5"
Velocity™ Expandable Interbody System
FDA UDI
Spine Wave, Inc.·10840642106794·Expandable Implant, 25(L) X 10(W) X 7-12(H), Bi...
TLIF/PLIF Disc Prep
FDA UDI
Life Spine, Inc.·00190837086879·
TrabecuLink Femoral and Tibial Cone - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575432219·Orthopaedic implant/instrument assembling devic...
K2M General Instruments
FDA UDI
VB Spine LLC·10888857531154·Screwdriver, Split Tip Size 383.5
H.M.T. ACUPUNCTURE NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
HEM-4030
FDA 510(k)
FDA Class 2
·Cardiovascular
CHARGER?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 17, 2025
CHARGER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 24, 2024
CHARGER?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 21, 2025
MOTO PARTIAL KNEE TIBIAL INSERT FIX S2 LM - 8MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSX·May 16, 2024
CHARGER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·June 2, 2025
CHARGER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 11, 2024
CHARGER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·March 27, 2025