ProSpore Biological Indicator

FDA registration

Mesa Laboratories Bozeman Manufacturing Facility (Zoot)·1 product·🇺🇸 United States

Crosstex International

FDA registration

Crosstex International·1 product·🇺🇸 United States

PROSPORE

FDA 510(k)

FDA Class 2 ·General Hospital

PEEK Corpectomy

FDA UDI

Nuvasive, Inc.·00887517623874·PEEK Corp Core, Ø14x32mm

KMEDIC

FDA UDI

TELEFLEX INCORPORATED·24026704293395·STEIN.PIN S.TROCAR 5" 3/32" 2.4MM (6PK)

Indicator, Biological Sterilization Process

FDA classification

FDA Class 2 ·Indicator, Biological Sterilization Process

SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE

FDA registration

Medtronic, Inc.·1 product·🇺🇸 United States

Sure-Flex Biliary Balloon Dilatation

FDA registration

SHENT CO., LTD. PLANT DIVISION·1 product·🇰🇷 South Korea

SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE

FDA registration

MEDTRONIC IRELAND·1 product·🇮🇪 Ireland

SilverHawk for Surgical Use

FDA registration

Medtronic, Inc.·1 product·🇺🇸 United States

Sureflex Biliary Balloon Dilatation

FDA registration

TeleMed Systems·1 product·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

T1007, Pointe Total Thyroxine (T4) Enzyme Immunoassay (EIA)

FDA registration

HORIBA INSTRUMENTS INCORPORATED·1 product·🇺🇸 United States

BTA TRAK Assay

FDA registration

POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC.·1 product·🇺🇸 United States

Siemens Multix TOP

FDA registration

CANUTE INTERNATIONAL MEDICAL SERVICES (CANADA) INC·1 product·🇨🇦 Canada

HICALIQ IVH BAG

FDA 510(k)

FDA Class 2 ·General Hospital

SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE

FDA 510(k)

FDA Class 2 ·Cardiovascular

Container, I.V.

FDA classification

FDA Class 2 ·Container, I.V.

Catheter, Peripheral, Atherectomy

FDA classification

FDA Class 2 ·Catheter, Peripheral, Atherectomy