17 results · 24ms · Sources: EU EUDAMED, US FDA

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SYNCHRON SYSTEMS OPIATES 2000 NG (OP2) REAGENT

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

Polystar HK

FDA UDI
Merz Dental GmbH·D7091984152·anteriors; shade A3.5; mould R 69

P.F.C.

FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295252429·P.F.C. TIBIAL INSERT FIXED BEARING CURVED 4 8mm...

MEDITHERM

FDA 510(k)
FDA Class 2 ·Physical Medicine

CENTURY COLOR TRACE

FDA 510(k)
FDA Class 2 ·Cardiovascular

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 13, 2013

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·January 8, 2014

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·May 12, 2015

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 6, 2012

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 24, 2013

BIA400 IMPLANT 4MM W ABUTMENT 8MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·May 25, 2016

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·April 1, 2013

ECHELON*FLEX60

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDW·February 10, 2011

MUSTANG¿

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·September 28, 2016

2.47MM X 30.3MM SPIRAL ROUTER

FDA Adverse Event
Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013

Depuy P.F.C. Modular Knee System, curved tibial insert (CVD); polyethylene tibial insert, Sz 4, 8.0 mm; Ref 98-4152.

FDA Recall
Terminated ·Depuy Orthopaedics, Inc.·Product code JWH·May 26, 2005

MENTOR MEMORYGEL XTRA BREAST IMPLANT

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·August 28, 2025