229 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Catalyst OrthoScience R1 Reverse Shoulder System
FDA 510(k)
FDA Class 2
·Orthopedic
NuVasive
FDA UDI
Nuvasive, Inc.·00195377046574·NTS Standard Tube, 26x110mm
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112960·CORNEAL TREPHINE BLADE8.75MM
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112809·BARRON VACUUM PUNCH 8.75MM
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668113288·STAB KNIFE 22.5 DEGREE (BX/5)
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
SIGNA MFO/I MAGNETIC RESONANCE SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
I-STAT ACT KAOLIN CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code JBP·May 20, 2026
AFFERA
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code QZI·February 23, 2026
I-STAT ACT KAOLIN CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code JBP·February 17, 2026
MICROSCAN KOVAC'S REAGENT
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code LQM·May 1, 2026
UNKNOWN INPEN
FDA Adverse Event
Malfunction
·COMPANION MEDICAL INC·Product code FMF·March 31, 2026
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø39/+3MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·July 22, 2022
630G INSULIN PUMP MMT-1715KR 630G
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·February 17, 2026
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 10, 2026
GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SIZE 4 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 31, 2022
OPEN ACCESS CAPIO
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FHQ·May 9, 2024
UNKNOWN NGP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 31, 2026
CADD CASSETTE 100ML W/FLOWSTOP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code LHI·April 15, 2022
STAR RF ELECTRODE
FDA Adverse Event
Malfunction
·STARMED CO.,LTD·Product code GEI·December 11, 2025