19 results · 42ms · Sources: EU EUDAMED, US FDA

ALTA Cervical Interbody Spacer

FDA registration
Astura Medical·1 product·🇺🇸 United States

Intervertebral fusion device with bone graft, cervical

FDA registration
ARCH Medical Solutions - Escondido LLC·1 product·🇺🇸 United States

CULVER TOOL & ENGINEERING

FDA registration
CULVER TOOL & ENGINEERING·1 product·🇺🇸 United States

ALTA Anterior Cervical Interbody Spacer

FDA 510(k)
FDA Class 2 ·Orthopedic

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486020279·MCK FEMORAL TEMPLATE (SIZE 4 RM/LL)

Zoll AED Plus

FDA registration
EMS SURPLUS CANADA·1 product·🇨🇦 Canada

Acero Precision

FDA registration
Acero Precision·1 product·🇺🇸 United States

Fixcet Spinal Facet Screw System

FDA registration
Xtant Medical Holdings, Inc.·1 product·🇺🇸 United States

LeMaitre Embolectomy Catheter

FDA UDI
Lemaitre Vascular, Inc.·00840663100613·5F 40 cm LeMaitre Embolectomy Catheter, eIFU

Denovo general purpose dental molar band

FDA UDI
Denovo Dental, Inc.·00810059290082·Denovo general purpose dental molar band - Maxi...

LeMaitre Embolectomy Catheter

FDA UDI
Lemaitre Vascular, Inc.·00840663100507·5F 40 cm LeMaitre Embolectomy Catheter

No Sting Skin Protectant, 28 mL

FDA registration
Sterigenics US LLC·3 products·🇺🇸 United States

B7551, Pointe Urea Nitrogen (BUN) (Berthelot/Colorimetric)

FDA registration
HORIBA INSTRUMENTS INCORPORATED·1 product·🇺🇸 United States

FIXCET SPINAL FACET SCREW SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

ZOLL AED PLUS WITH 2010 AHA GUIDLINES SOFTWARE UPDATE

FDA 510(k)
FDA Class 3 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical

YANKAUER SUCTION SET- STANDARD TIP/WITHOUT VACUUM CONTROL- SP-2M - 160 161

FDA registration
PLASTI-MED PLASTIK MEDIKAL URUNLER SAN. VE TIC. LTD. STI.·1 product·🇹🇷 Türkiye

System, Facet Screw Spinal Device

FDA classification
FDA Unclassified ·System, Facet Screw Spinal Device

Automated External Defibrillators (Non-Wearable)

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