59 results · 25ms · Sources: EU EUDAMED, 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