Synergy Health Marseille SAS

FDA registration

Synergy Health Marseille SAS·1 product·🇫🇷 France

STERISPINE LC Lumbar Interbody Device

FDA registration

SAFE ORTHOPAEDICS SAS·1 product·🇫🇷 France

STERISPINE LC CAGE

FDA 510(k)

FDA Class 2 ·Orthopedic

ArgenZ HT+ 98x14 C3

FDA UDI

ARGEN CORPORATION, THE·D818122021·Dental porcelain/ceramic restoration kit

Partial Thromboplastin (APT) Reagent

FDA registration

SANZAY CORPORATION -·1 product·🇺🇸 United States

ACTIVATED PARTIAL THROMBOPLASTIN

FDA registration

TECO DIAGNOSTICS·1 product·🇺🇸 United States

INOmax DSIR (Delivery System)

FDA registration

Mallinckrodt Manufacturing LLC·3 products·🇺🇸 United States

QuickCoag APTT-EA

FDA registration

BIOMEDICA DIAGNOSTICS INC.·1 product·🇨🇦 Canada

75V - Class A 21 - 3 Shelf Cabinet

FDA UDI

Certified Safety Manufacturing, Inc.·00766588620213·75V - Class A 21 - 3 Shelf Cabinet

BioHorizons

FDA UDI

BIOHORIZONS IMPLANT SYSTEMS, INC·00847236000974·2.0 x 21mm CGS Pilot Drill

Cuff pressure manometer

FDA registration

MEDLINE INDUSTRIES, LP - Northfield·1 product·🇺🇸 United States

SPARTRONICS STRONGSVILLE, INC.

FDA registration

SPARTRONICS STRONGSVILLE, INC.·1 product·🇺🇸 United States

CRYO-TOUCH II

FDA 510(k)

FDA Class 2 ·Neurology

VITAL SCIENTIFIC APTT, APTT & QUIKCOAG APTT

FDA 510(k)

FDA Class 2 ·Hematology

Device, Surgical, Cryogenic

FDA classification

FDA Class 2 ·Device, Surgical, Cryogenic

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Activated Partial Thromboplastin

FDA classification

FDA Class 2 ·Activated Partial Thromboplastin