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