28 results · 21ms · Sources: EU EUDAMED, US FDA

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4635 ASSISTANT'S INSTRUMENTATION

FDA 510(k)
FDA Class 1 ·Dental

PowerPICC Provena SOLO

FDA UDI
Bard Access Systems, Inc.·00801741202063·Catheter Placement Kit

Preat

FDA UDI
Preat Corporation·00842092165867·NobelActive™/Conical-compatible RP Titanium Bla...

AtriClip® LAA Exclusion System

FDA UDI
ATRICURE, INC.·00818354015058·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...

Epredia

FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693214360·Cassettes are designed to contain incised tissu...

AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion System

FDA UDI
ATRICURE, INC.·10840143912085·LAA Exclusion System, PRO245

AtriClip® LAA Exclusion System

FDA UDI
ATRICURE, INC.·10840143900198·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...

AtriClip® LAA Exclusion System

FDA UDI
ATRICURE, INC.·10840143907418·AtriClip® PRO2 Gillinov-Cosgrove LAA Exclusion ...

Preat Implant Prosthetics

FDA UDI
Preat Corporation·00842092165874·NobelActive™/Conical-compatible RP – Milled Ti...

REF SHADE

FDA UDI
AMERICAN TOOTH INDUSTRIES·D772ATI250009670·3-OZ REF SH-67 TOOTH SHADE COLD CU

SECURMIX

FDA 510(k)
FDA Class 2 ·General Hospital

ALKALINE PHOSPHATASE LIQUID REAGENT-KINETIC, MODELS A504-150 AND A504-500H

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

ANESTAR

FDA Adverse Event
Malfunction ·MINDRAY DS USA, INC.·Product code BSZ·March 30, 2009

6800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 27, 2013

PRECISION

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 18, 2011

CONTEGRA PULMONARY VALVED CONDUIT

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES, INC.·Product code MWH·February 15, 2008

Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

FDA Recall
Open, Classified ·Preat Corp·Product code NHA·February 9, 2024

BD TRUCOUNT TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 13, 2021

Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

FDA Enforcement
Class II ·Ongoing·Preat Corp·March 27, 2024

BD TRUCOUNT TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code GKZ·July 15, 2021