XSTAT 30 Generation 2

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

XSTAT 30 Generation 2

FDA registration

REVMEDX, INC.·2 products·🇺🇸 United States

XSTAT 30, 1-Pack

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Non-Absorbable, Expandable, Hemostatic Sponge For Temporary Internal Use

FDA classification

FDA Class 2 ·Non-Absorbable, Expandable, Hemostatic Sponge For Temporary Internal Use

FINN KNEE SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304268968·

ProFil

FDA UDI

SILMET LTD·07290015358521·Dental Composite Restorative

PFT Kit A

FDA UDI

A-M SYSTEMS, LLC·00817081021202·PFT Kit A, 35mm Kit Case

611 - ANKLE FUSION NAIL

FDA registration

IONISOS·1 product·🇫🇷 France

Sodium Chloride Inhalation Solution, USP 3%, 7%, and 10%

FDA registration

NEPHRON SC, LLC.·1 product·🇺🇸 United States

Ophthalmic Retractor

FDA UDI

KATENA PRODUCTS, INC.·00841668100943·JAFFE LID RETRACTOR SMALL

Gastrointestinal Pathogen Panel (GPP) Kit

FDA registration

Applied BioCode, Inc.·2 products·🇺🇸 United States

UltraCor Twirl Needle

FDA registration

ARMOR PLAST LTD·1 product·🇮🇳 India

Crescent™ Jugular Dual Lumen Catheter

FDA registration

MC3, Inc.·1 product·🇺🇸 United States

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361009900·PedFuse ReTurn, SLD, 9.0mm x 70mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361009856·PedFuse ReTurn, SLD, 9.0mm x 45mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361009924·PedFuse ReTurn, SLD, 9.0mm x 80mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361009863·PedFuse ReTurn, SLD, 9.0mm x 50mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361009917·PedFuse ReTurn, SLD, 9.0mm x 75mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361009894·PedFuse ReTurn, SLD, 9.0mm x 65mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361009825·PedFuse ReTurn, SLD, 9.0mm x 30mm