46 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RESTORIS POROUS PARTIAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526814721·GENUMEDI PSS GREEN O
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526768451·GENUMEDI PSS GREEN I
HLS Plate, Straight
FDA UDI
I.T.S. GmbH·09120047304693·HLS Plate, Straight, 1.0mm, 10-Hole, Left
PIEZOELECTRIC SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HES ULTRASONIC THERAPY APPLIANCE, MODELS HS-3008 (1MHZ), HS3026 (2MHZ), HS-3040 (3MHZ)
FDA 510(k)
FDA Class 2
·Physical Medicine
Widex
FDA UDI
Widex A/S·05706069655537·Widex UNIQUE U-IM (Clay brown ) 110, Right
Widex
FDA UDI
Widex A/S·05706069887471·WIDEX MOMENT M-IM (Light beige ) 110, Right
Widex
FDA UDI
Widex A/S·05706069887495·WIDEX MOMENT M-IM (Dark brown ) 110, Right
Widex
FDA UDI
Widex A/S·05706069887488·WIDEX MOMENT M-IM (Clay brown ) 110, Right
Widex
FDA UDI
Widex A/S·05706069655520·Widex UNIQUE U-IM (Light beige ) 110, Right
Widex
FDA UDI
Widex A/S·05706069655544·Widex UNIQUE U-IM (Dark brown ) 110, Right
CAPD SOLUTION TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 6, 2011
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 6, 2013
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 5, 2008
OSS TIBIAL POLY BEARING 12MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·June 17, 2019
OSS POLY LOCK PIN
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·June 17, 2019
INTELLIVUE MULTI-MEASUREMENT MODULE X3
FDA Adverse Event
Malfunction
·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·June 12, 2025
OSS 5CM DIAPHYSEAL SEGMENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·October 3, 2019
OSS POLY TIBIAL BUSHING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·April 11, 2023