46 results · 24ms · Sources: EU EUDAMED, 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