59 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Midas Touch-Nitrile Examination Gloves- Powder free, Orange, XS, Model SNAEFT-240OR-XS; Midas Touch-Nitrile Examination Gloves -Powder free, Orange, XXL, Model SNAEFT-240OR-XXL
FDA 510(k)
FDA Class 1
·General Hospital
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526768482·GENUMEDI PSS GREEN IV
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304006492·
AGXO
FDA UDI
Oticon A/S·05707131288578·H110V2, DESIGNRITE 10 WL SGR AGXO
MAXIIa
FDA UDI
Aei Technologies, Inc.·B9671504140·Metabolic Measurement System
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100073·TEMPORAL SPECULUM SOLID BLADES
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100127·KRATZ-BARRAQUER SPECULUM RIGHT EYE
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962104743·NEATCUT BLADE, 3.5MM, S
PROTOE ENDOSORB SMALL HAMMER TOE PIN
FDA 510(k)
FDA Class 2
·Orthopedic
PLIX
FDA 510(k)
FDA Class 2
·Anesthesiology
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962102756·DISPOSABLE ARTHROSCOPIC 3.5mm NEATCUT SHAVER BL...
PRODIGY AUTOCODE
FDA Adverse Event
Injury
·OK BIOTECH CO., LTD.·Product code NBW·May 4, 2016
ORTHOPEDIC SALVAGE SYSTEM (OSS) BUMPER LOCKING PIN
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KRO·December 2, 2016
ORTHOPEDIC SALVAGE SYSTEM (OSS) YOKE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KRO·December 2, 2016
SOLYX SIS SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 6, 2013
JOSTRA
FDA Adverse Event
Malfunction
·MAQUET, INC·Product code DTR·June 21, 2011
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 5, 2008
OSS TIBIAL AUGMENT BLOCK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·June 9, 2017
OSS TIBIAL AUGMENT BLOCK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·June 9, 2017
Knee Products: 150414 Orthopedic Salvage System (OSS) Tibial Bearing, 20 MM Standard - Product Usage: Knee prosthesis
FDA Recall
Terminated
·Biomet, Inc.·Product code JDI·April 17, 2020