54 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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36M - MSHA Miners
FDA UDI
Certified Safety Manufacturing, Inc.·00766588026206·36M - MSHA Miners
FlexCath Advance Steerable Sheath and Dilator
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
Synthes GmbH·10886982144317·3.0MM CANNULATED SCREW SHORT THREAD/20MM
Marking Pen
FDA UDI
KATENA PRODUCTS, INC.·00841668113219·MARKING PEN FOR TREPHINE & PUNCH
Medical Facets NC
FDA UDI
MEDICAL FACETS NC LLC·M933MDF2026200·3.0mm Cannulated Screw, Short Thread, 20mm
Diamond Orthopedic, LLC
FDA UDI
DIAMOND ORTHOPEDIC, LLC·B551DMD2026200·3.0mm, Cannulated Screw, Short Thd., 20mm
SHEATHLESS ACCESSORY KIT, MODELS XRIK24, XRIK28, XRIK32, XRIK36, XRIK40 AND XRIKRT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SURESMILE SYSTEM
FDA 510(k)
FDA Class 1
·Dental
HEPARIN GRAFTED (EVODIAL)
FDA Adverse Event
Malfunction
·VANTIVE US HEALTHCARE LLC·Product code KDI·April 16, 2026
I-STAT CHEM8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JPI·February 10, 2026
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 18, 2026
PUMP 1886 780G OUS BLE PUMP MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 25, 2026
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 4, 2026
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 3, 2026
POWERGLIDE PRO
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code FOZ·May 5, 2026
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 6, 2026
STOCKERT CENTRIFUGAL PUMP CONSOLE
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code KFM·October 15, 2014
OMNISPAN MENISCAL FASTENER, 12 DEGREE
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code MBI·August 11, 2011
PINN 100 W/GRIPTION 52MM
FDA Adverse Event
Injury
·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·July 2, 2013
MMT-712 PARADIGM INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·January 22, 2026