VALO Grand

FDA registration

Ultradent Products Inc. / OraTech LLC·1 product·🇺🇸 United States

VALO Grand

FDA 510(k)

FDA Class 2 ·Dental

N/A

FDA UDI

GEORGE TIEMANN & CO.·B5821605510·FORCEPS

Activator, Ultraviolet, For Polymerization

FDA classification

FDA Class 2 ·Activator, Ultraviolet, For Polymerization

Radial

FDA registration

INSITU TECHNOLOGIES, INC.·1 product·🇺🇸 United States

Synergy Health Ireland Ltd

FDA registration

Synergy Health Ireland Ltd·1 product·🇮🇪 Ireland

BRIVANT, LTD.

FDA registration

BRIVANT, LTD.·1 product·🇮🇪 Ireland

ORLocate Sponge System

FDA registration

STERIS CORPORATION·1 product·🇺🇸 United States

Synergy Health Sterilisation UK Ltd

FDA registration

Synergy Health Sterilisation UK Ltd·1 product·🇬🇧 United Kingdom

IN-OVATION® C

FDA UDI

DENTSPLY SIRONA ORTHODONTICS INC.·D807K100551821·IN-OVATION® C EURO 018 U5-5/L3-3 CS-BC HK

N/A

FDA UDI

DENTSPLY SIRONA ORTHODONTICS INC.·D807K100551921·In-Ovation C/R RNC/BASE/EURO 018 UL5-5 CS-BC HK

IN-OVATION® C

FDA UDI

DENTSPLY SIRONA ORTHODONTICS INC.·D807K100551811·IN-OVATION® C EURO 018 U5-5/L3-3 CS HK

Disposable CryoProbe

FDA registration

Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium

CX50N(CX50YQS)

FDA registration

WIDE USA CORPORATION·1 product·🇺🇸 United States

BLAZEJEWSKI MEDI-TECH GMBH

FDA registration

BLAZEJEWSKI MEDI-TECH GMBH·1 product·🇩🇪 Germany

Cryo Probe: Extended Retinal, 2.5mm

FDA registration

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.·1 product·🇳🇱 Netherlands

BRIVANT GUIDEWIRE

FDA 510(k)

FDA Class 2 ·Cardiovascular

ORLOCATE SYSTEM MODEL ORL 100

FDA 510(k)

FDA Class 1 ·General Hospital

Counter, Sponge, Surgical

FDA classification

FDA Class 1 ·Counter, Sponge, Surgical

Wire, Guide, Catheter

FDA classification

FDA Class 2 ·Wire, Guide, Catheter