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

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SYNTHES CALCANEAL PLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756001397·Cervical Collar

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·10304040051389·FILE - Channels PT Platinum 25MM Assortment - G...

BUSCH®, BNA®

FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120204011·Carbide - Excavating and fissure burs

I-SIL Heavy Body Regular Set

FDA UDI
Spident Co., Ltd.·08809262955033·Vinyl Polysiloxane Impression Material

Large Hex Driver Cann Hud-Mod

FDA UDI
Osteocentric Technologies, Inc.·00810097801127·Large Hex Driver Cann Hud-Mod

Midway Select

FDA UDI
MIDWAY DENTAL SUPPLY, LLC·10843717103964·Stainless Steel K Files (Hand), Size # 40, Leng...

BESTWAY PRODUCTS

FDA registration
BESTWAY PRODUCTS·1 product·🇺🇸 United States

EASYMIX® vacuum pump I

FDA UDI
OSARTIS GmbH·04260056881633·The devices are used with an EASYMIX® vacuum mi...

RADIESSE

FDA Adverse Event
Injury ·MERZ NORTH AMERICA, INC (FRANKSVILLE)·Product code LMH·June 25, 2025

Keos Anterior Cervical Case/Caddy

FDA UDI
KEOS·B0842020204010·

CIDEX OPA SOLUTION (0.55% ORTHRO-PHTHALALDEHYDE SOLUTION)

FDA 510(k)
FDA Class 2 ·General Hospital

VAPOTHERM, MODEL 2000I

FDA 510(k)
FDA Class 2 ·Anesthesiology

CERENOVUS ENTERPRISE

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SARL·Product code NJE·January 19, 2026

VIDAS® CMV IGG ASSAY

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code LFZ·September 5, 2019

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013

LC PCA III INFUSER

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code MEA·February 8, 2011

CARPENTIER-EDWARDS PERIMOUNT MAGNA AORTIC BIOPROSTHESIS

FDA Adverse Event
Death ·EDWARDS LIFESCIENCES·Product code LWR·March 26, 2008

VIDAS® CMV IGG

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code LFZ·February 19, 2019

VIDAS® CMV IGG

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code LFZ·February 8, 2019