24 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CIRRUS HD-OCT
FDA 510(k)
FDA Class 2
·Ophthalmic
X-CORE
FDA UDI
Nuvasive, Inc.·00887517300928·X-CORE 2 Ti Endcap, 22mm Rnd 0° Ø18
X-CORE
FDA UDI
Nuvasive, Inc.·00887517434685·X-CORE 2 Ti Endcap, 22mm Rnd 0° Ø22
FLEXIBLE REAMER SHAFT 2.0mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665023688·
G185
FDA UDI
RESEARCH INSTRUMENTS LIMITED·05060554120109·Incubator for assisted reproduction
G185
FDA UDI
RESEARCH INSTRUMENTS LIMITED·05060554120116·Incubator for assisted reproduction
FLEXIBLE SHAFT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·March 6, 2025
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102099·R Tibial Baseplate Cemented Keeled Sz 2
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101320·R Tibial Baseplate Cemented Stemmed Sz 2 Insert A
A3F FRATIONAL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PENTRA 120/PENTRA 120 RETIC OPTIONS SPS, MODEL PENTRA 120
FDA 510(k)
FDA Class 2
·Hematology
FLEXIBLE SHAFT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·August 25, 2025
Truliant
FDA UDI
Exactech, Inc.·10885862523747·TRULIANT POROUS TAMP HEAD
FLEXIBLE SHAFT
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·December 5, 2025
FLEXIBLE REAMER SHAFT, 2.0MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·September 14, 2021
BIOMET SERIES A STANDARD PATELLA 28MM X 8.0MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·August 24, 2011
OXIMAX N-560 PULSE OXIMETER
FDA Adverse Event
Malfunction
·MEDIANA·Product code DQA·November 3, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 12, 2013
NEEDLE FILTER BLUNT FILL 18X1-1/2
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·February 28, 2020
TRUE METRIX
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH INC·Product code NBW·July 1, 2020