PerioGlas Bioactive Synthetic Bone Graft Particulate

FDA registration

NOVABONE PRODUCTS, LLC·1 product·🇺🇸 United States

NovaBone Dental Morsels

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

NOVABONE DENTAL MORSELS - BIOACTIVE SYNTHETIC BONE GRAFT

FDA 510(k)

FDA Class 2 ·Dental

BUCK

FDA UDI

Smith & Nephew, Inc.·03596010041968·BUCK FEMORAL CEMENT RESTRICTOR INSERTER

LifePak 500 AED

FDA registration

EMS SURPLUS CANADA·1 product·🇨🇦 Canada

GlamaComp

FDA registration

SPIDENT CO., LTD.·1 product·🇰🇷 South Korea

Bone Grafting Material, Synthetic

FDA classification

FDA Class 2 ·Bone Grafting Material, Synthetic

ProLift

FDA UDI

Life Spine, Inc.·00190837116545·

ProLift

FDA UDI

Life Spine, Inc.·00190837093303·

ProLift Lateral

FDA UDI

Life Spine, Inc.·00190837104641·

ANTISERA, LATEX AGGLUTINATION, CRYPTOCOCCUS NEOFORMANS

FDA registration

MONOCENT INC.·1 product·🇺🇸 United States

Sterigenics U.S., LLC

FDA registration

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

Isopure Sodium Bicarbonate Mixing and Distribution System

FDA registration

ISOPURE, CORP.·1 product·🇺🇸 United States

WUNDER TEST

FDA 510(k)

FDA Class 2 ·Clinical Toxicology

MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA 510(k)

FDA Class 3 ·Cardiovascular

Gibralt

FDA UDI

Choice Spine, LP·00840996169455·GIBRALT,DRILL,FIXED,2.4X28

Enzyme Immunoassay, Cannabinoids

FDA classification

FDA Class 2 ·Enzyme Immunoassay, Cannabinoids

Automated External Defibrillators (Non-Wearable)

FDA classification

FDA Class 3 ·Automated External Defibrillators (Non-Wearable)