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

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VULCAN ELECTROSURGICAL PROBES: VULCAN MICRO LIGAMENT CHISELS, VULCAN LIGAMENT CHISELS, VULCAN EFLEX LIGAMENT CHISELS

FDA 510(k)
FDA Class 2 ·Orthopedic

Nobel

FDA UDI
Preat Corporation·00842092101377·NobelBiocare™ Tri-Lobe-compatible WP Snappy Abu...

PowerPICC Provena

FDA UDI
Bard Access Systems, Inc.·00801741136597·Catheter Placement Kit

AtriClip™ LAA Exclusion System

FDA UDI
ATRICURE, INC.·10840143906183·AtriClip® Gilinov-Cosgrove LAA Exclusion System 50

S NEEDLE

FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282505448·asia-med s-needle J-Type 3050 Place N' Press: c...

AtriClip® Gillinov-Cosgrove® LAA Exclusion System

FDA UDI
ATRICURE, INC.·10840143911934·LAA Exclusion System, ACH150

AtriClip™ LAA Exclusion System

FDA UDI
ATRICURE, INC.·10840143900082·AtriClip® Gilinov-Cosgrove LAA Exclusion System 50

S NEEDLE

FDA UDI
asia-med GmbH·04251282512439·asia-med s-needle J-Type 3050 Place N' Press: c...

AtriClip™ LAA Exclusion System

FDA UDI
ATRICURE, INC.·00818354011449·AtriClip® Gilinov-Cosgrove LAA Exclusion System 50

AtriClip® Gillinov-Cosgrove™ LAA Exclusion System

FDA UDI
ATRICURE, INC.·10840143913358·LAA Exclusion System, ACH150

FlowLogic Assert

FDA UDI
SONENDO, INC.·00810209420956·FlowLogic Assert Shaping File .04 Kit, 25mm

MFCD 118

FDA 510(k)
FDA Class 2 ·Radiology

DURACON SYMMETRIC METAL-BACKED PATELLAR COMPONENT

FDA 510(k)
FDA Class 2 ·Orthopedic

PLATE BD CHROMAGAR O-157 20 EA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JSI·August 10, 2021

PLATE BD CHROMAGAR O-157 20 EA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JSI·August 10, 2021

OPTETRAK

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·August 6, 2019

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·March 12, 2013

VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC IGM REAGENT

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LOM·February 24, 2011

COBAS INTEGRA 800

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 15, 2008

OMNIPOD INSULIN MANAGEMENT SYSTEM

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·November 15, 2019