27 results
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26ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Urethrotech UCD
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ATLANTIS® Anterior Cervical Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000867928·PLATE 6190060 ANTERIOR CERVICAL 60MM
ATLANTIS® Anterior Cervical Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994235688·PLATE 6190060 ANTERIOR CERVICAL 60MM
Jawz Endomyocardial Biopsy Forceps
FDA UDI
ARGON MEDICAL DEVICES, INC.·00886333206759·Jawz Endomyocardial Biopsy Forceps 6F x 50cm St...
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101056·KNAPP RETRACTOR 4-PRONG BLUNT
Mariner Cortical
FDA UDI
Seaspine Orthopedics Corporation·10889981169473·CORTICAL SHANK, Cannulated, 9.0 X 60
Mariner Cortical
FDA UDI
Seaspine Orthopedics Corporation·10889987169477·CORTICAL SHANK, Cannulated, 9.0 X 60
Coral
FDA UDI
Seaspine Orthopedics Corporation·10889981029081·Prebent Rod 5.5 x 60
EON 100 CHEMISTRY ANALYZER WITH ISE , MODEL 77105, BICARBONATE REAGENT, MODEL 77475
FDA 510(k)
FDA Class 2
·Clinical Chemistry
NEXLINK OCT SYSTEM, MODEL 7000 SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
BIOLOX DELTA CER LNR 36MM E
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·February 5, 2026
RINGLOC-X E1 H/W 56/36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·April 27, 2026
BIOLOX DELTA CER LNR 40MM G
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·April 27, 2026
PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·October 6, 2008
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013
INRATIO2
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·June 29, 2011
AVAN E1 INSERT 28 S 52
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·March 6, 2025
BIOLOX DELTA CER LNR 32MM E
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·September 8, 2025
RINGLOC BIPOLAR VIVACIT-E
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·September 10, 2025
BIOLOX DELTA CER LNR 36MM E
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·November 13, 2025