77 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Novapak Nasal Sinus Packing and Stent
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704513929·
NA
FDA UDI
Synthes GmbH·10886982144348·3.0MM CANNULATED SCREW SHORT THREAD/23MM
36M - MSHA Miners
FDA UDI
Certified Safety Manufacturing, Inc.·00766588026206·36M - MSHA Miners
Diamond Orthopedic, LLC
FDA UDI
DIAMOND ORTHOPEDIC, LLC·B551DMD2026230·3.0mm, Cannulated Screw, Short Thd., 23mm
Medical Facets NC
FDA UDI
MEDICAL FACETS NC LLC·M933MDF2026230·3.0mm Cannulated Screw, Short Thread, 23mm
ABSORBENT PAPER POINTS
FDA UDI
DiaDent Group International·08806383513418·"An absorbent paper points is an endodontic pap...
5.0 MM DIAMETER POLYAXIAL SCREWS (MOSS MIAMI 6.35MM SYSTEM)
FDA 510(k)
FDA Class 2
·Orthopedic
PURESPERM 40 AND PURESPERM 80
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ABL90 FLEX PLUS ANALYZER
FDA Adverse Event
Malfunction
·RADIOMETER MEDICAL APS·Product code CHL·March 12, 2026
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 27, 2026
ABL90 FLEX PLUS ANALYZER
FDA Adverse Event
Malfunction
·RADIOMETER MEDICAL APS·Product code CHL·March 12, 2026
PUMP 1886 780G OUS BLE PUMP MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 27, 2026
I-STAT TROPONIN (HS-TNI ) CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code MMI·April 14, 2026
PUMP 1886 780G OUS BLE PUMP MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 28, 2026
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 27, 2026
MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 29, 2026
CAPTURE-R READY SCREEN
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·October 21, 2008
V.A.C. THERAPY SYSTEM
FDA Adverse Event
Death
·KCI USA, INC.·Product code OMP·August 4, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013